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nsv4372558

  • Variant Calls:36
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,830

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1327 SVs from 93 studies. See in: genome view    
Remapped(Score: Perfect):1,690,335-1,741,164Question Mark
Overlapping variant regions from other studies: 1344 SVs from 93 studies. See in: genome view    
Submitted genomic1,621,774-1,672,603Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4372558RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr11,690,3351,741,164
nsv4372558Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr11,621,7741,672,603

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15612429copy number loss1-0669-003SNP arrayGenotyping24
nssv15616458copy number loss1-0825-003SNP arrayGenotyping22
nssv15616848copy number loss1-0811-003SNP arrayGenotyping22
nssv15617529copy number loss1-0153-002SNP arrayGenotyping25
nssv15618083copy number loss1-0883-003SNP arrayGenotyping18
nssv15625776copy number loss1-0375-001SNP arrayGenotyping19
nssv15627567copy number loss1-0489-003SNP arrayGenotyping13
nssv15627580copy number loss1-0489-004SNP arrayGenotyping18
nssv15628303copy number loss1-0513-004SNP arrayGenotyping19
nssv15629221copy number loss1-0566-003SNP arrayGenotyping21
nssv15632230copy number loss10-1090-004SNP arrayGenotyping26
nssv15637222copy number loss12-8115-001SNP arrayGenotyping18
nssv15637459copy number loss13-0095-004SNP arrayGenotyping24
nssv15638055copy number loss14-0063-003SNP arrayGenotyping21
nssv15639692copy number loss14-0144-004SNP arrayGenotyping18
nssv15643592copy number loss2-0003-003SNP arrayGenotyping18
nssv15645562copy number loss2-0305-002SNP arrayGenotyping30
nssv15646423copy number loss2-1186-002SNP arrayGenotyping16
nssv15652777copy number loss2-1540-003SNP arrayGenotyping28
nssv15655921copy number loss2-1749-003SNP arrayGenotyping19
nssv15657534copy number loss4-0028-002SNP arrayGenotyping25
nssv15658662copy number loss3-0544-000SNP arrayGenotyping17
nssv15658679copy number loss3-0546-000SNP arrayGenotyping15
nssv15661064copy number loss4-0071-003SNP arrayGenotyping19
nssv15662360copy number loss4-0083-003SNP arrayGenotyping20
nssv15662711copy number loss5-0134-001SNP arrayGenotyping23
nssv15663862copy number loss5-0140-002SNP arrayGenotyping24
nssv15666308copy number loss5-0124-002SNP arrayGenotyping25
nssv15667441copy number loss5-0124-003SNP arrayGenotyping21
nssv15667586copy number loss5-0148-003SNP arrayGenotyping23
nssv15671469copy number loss7-0308-003SNP arrayGenotyping30
nssv15679805copy number loss208585SNP arrayGenotyping15
nssv15696093copy number loss155473SNP arrayGenotyping18
nssv15697047copy number loss127822SNP arrayGenotyping26
nssv15701392copy number loss79240SNP arrayGenotyping12
nssv15702182copy number loss201483SNP arrayGenotyping17

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15612429RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15616458RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15616848RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15617529RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15618083RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15625776RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15627567RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15627580RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15628303RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15629221RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15632230RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15637222RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15637459RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15638055RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15639692RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15643592RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15645562RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15646423RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15652777RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15655921RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15657534RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15658662RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15658679RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15661064RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15662360RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15662711RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15663862RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15666308RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15667441RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15667586RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15671469RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15679805RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15696093RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15697047RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15701392RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15702182RemappedPerfectNC_000001.11:g.(?_
1690335)_(1741164_
?)del
GRCh38.p12First PassNC_000001.11Chr11,690,3351,741,164
nssv15612429Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15616458Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15616848Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15617529Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15618083Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15625776Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15627567Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15627580Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15628303Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15629221Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15632230Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15637222Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15637459Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15638055Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15639692Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15643592Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15645562Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15646423Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15652777Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15655921Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15657534Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15658662Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15658679Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15661064Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15662360Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15662711Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15663862Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15666308Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15667441Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15667586Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15671469Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15679805Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15696093Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15697047Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15701392Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603
nssv15702182Submitted genomicNC_000001.10:g.(?_
1621774)_(1672603_
?)del
GRCh37 (hg19)NC_000001.10Chr11,621,7741,672,603

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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