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nsv4383205

  • Variant Calls:42
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,562

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 934 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):11,068,228-11,094,789Question Mark
Overlapping variant regions from other studies: 935 SVs from 85 studies. See in: genome view    
Submitted genomic11,220,827-11,247,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4383205RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1211,068,22811,094,789
nsv4383205Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1211,220,82711,247,388

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15614530copy number loss1-0135-003SNP arrayGenotyping32
nssv15615040copy number gain1-0139-001SNP arrayGenotyping17
nssv15615795copy number gain1-0786-003SNP arrayGenotyping19
nssv15617133copy number loss1-0763-005SNP arrayGenotyping18
nssv15617470copy number gain1-0820-003SNP arrayGenotyping18
nssv15617752copy number gain1-0153-005SNP arrayGenotyping15
nssv15625329copy number loss1-0318-004SNP arrayGenotyping20
nssv15626410copy number loss1-0051-006SNP arrayGenotyping32
nssv15629034copy number loss1-0548-001SNP arrayGenotyping20
nssv15636445copy number gain13-0053-002SNP arrayGenotyping20
nssv15637147copy number loss12-4855-002SNP arrayGenotyping26
nssv15641059copy number loss14-0349-004SNP arrayGenotyping21
nssv15641640copy number loss14-0243-002SNP arrayGenotyping15
nssv15649229copy number gain2-1266-002SNP arrayGenotyping24
nssv15650706copy number gain2-1362-004SNP arrayGenotyping15
nssv15651914copy number gain2-1620-002SNP arrayGenotyping27
nssv15654070copy number loss2-1690-002SNP arrayGenotyping24
nssv15657637copy number loss4-0039-003SNP arrayGenotyping21
nssv15660209copy number loss3-0657-000SNP arrayGenotyping16
nssv15661712copy number gain4-0034-001SNP arrayGenotyping17
nssv15664667copy number loss4-0078-003SNP arrayGenotyping17
nssv15665615copy number gain7-0081-003SNP arrayGenotyping21
nssv15668369copy number gain7-0192-003SNP arrayGenotyping19
nssv15668772copy number loss7-0227-003SNP arrayGenotyping17
nssv15670060copy number gain7-0255-003SNP arrayGenotyping24
nssv15670107copy number loss7-0257-003SNP arrayGenotyping18
nssv15673750copy number gain227577SNP arrayGenotyping17
nssv15677910copy number gain222678SNP arrayGenotyping18
nssv15679288copy number gain208022SNP arrayGenotyping13
nssv15680788copy number gain227579SNP arrayGenotyping16
nssv15680894copy number loss232713SSNP arrayGenotyping24
nssv15681962copy number gain211606SNP arrayGenotyping23
nssv15684027copy number lossOCD147-DS-1432SNP arrayGenotyping22
nssv15685122copy number lossOCD165-8961162SNP arrayGenotyping21
nssv15689269copy number lossOCD10-S_896171SNP arrayGenotyping23
nssv15689376copy number gainOCD100-1572SNP arrayGenotyping19
nssv15689558copy number lossOCD111-S_1657SNP arrayGenotyping25
nssv15691846copy number gainOCD80-896742SNP arrayGenotyping19
nssv15693219copy number gainOCD88-0625-0648-2SNP arrayGenotyping18
nssv15694538copy number lossOCD98-1525SNP arrayGenotyping23
nssv15699740copy number gain226265SNP arrayGenotyping20
nssv15701622copy number gain223694SNP arrayGenotyping20

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15614530RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15615040RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15615795RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15617133RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15617470RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15617752RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15625329RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15626410RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15629034RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15636445RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15637147RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15641059RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15641640RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15649229RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15650706RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15651914RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15654070RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15657637RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15660209RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15661712RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15664667RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15665615RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15668369RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15668772RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15670060RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15670107RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15673750RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15677910RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15679288RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15680788RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15680894RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15681962RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15684027RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15685122RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15689269RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15689376RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15689558RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15691846RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15693219RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15694538RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15699740RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15701622RemappedPerfectNC_000012.12:g.(?_
11068228)_(1109478
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,068,22811,094,789
nssv15614530Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15615040Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15615795Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15617133Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15617470Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15617752Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15625329Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15626410Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15629034Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15636445Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15637147Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15641059Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15641640Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15649229Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15650706Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15651914Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15654070Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15657637Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15660209Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15661712Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15664667Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15665615Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15668369Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15668772Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15670060Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15670107Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15673750Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15677910Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15679288Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15680788Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15680894Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15681962Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15684027Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15685122Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15689269Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15689376Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15689558Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15691846Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15693219Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15694538Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15699740Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388
nssv15701622Submitted genomicNC_000012.11:g.(?_
11220827)_(1124738
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,220,82711,247,388

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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