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nsv4372963

  • Variant Calls:40
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:73,410

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 374 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):50,070,587-50,143,996Question Mark
Overlapping variant regions from other studies: 293 SVs from 53 studies. See in: genome view    
Submitted genomic51,830,347-51,903,756Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4372963RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1050,070,58750,143,996
nsv4372963Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1051,830,34751,903,756

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15618924copy number loss1-0895-003SNP arrayGenotyping16
nssv15619038copy number loss1-0181-001SNP arrayGenotyping15
nssv15627383copy number loss1-0539-002SNP arrayGenotyping22
nssv15628515copy number loss1-0551-004SNP arrayGenotyping23
nssv15630764copy number loss1-0621-003SNP arrayGenotyping19
nssv15633287copy number loss11-0017-003SNP arrayGenotyping14
nssv15641191copy number loss14-0286-001SNP arrayGenotyping16
nssv15644673copy number loss16-1000-003SNP arrayGenotyping23
nssv15646536copy number loss2-1268-002SNP arrayGenotyping29
nssv15653120copy number loss2-1623-002SNP arrayGenotyping17
nssv15658971copy number loss4-0056-002SNP arrayGenotyping23
nssv15660544copy number loss5-0006-003SNP arrayGenotyping24
nssv15660604copy number loss5-0008-001SNP arrayGenotyping22
nssv15664084copy number loss231670SNP arrayGenotyping14
nssv15670263copy number loss7-0291-003SNP arrayGenotyping23
nssv15671500copy number loss7-0309-003SNP arrayGenotyping21
nssv15672725copy number loss7-0336-003SNP arrayGenotyping16
nssv15674838copy number loss209356SNP arrayGenotyping25
nssv15676373copy number loss209352SNP arrayGenotyping33
nssv15682633copy number lossOCD121-S_1737SNP arrayGenotyping25
nssv15682747copy number lossOCD1130-5299SNP arrayGenotyping19
nssv15684204copy number lossOCD112-B_1664SNP arrayGenotyping19
nssv15684311copy number lossOCD1137-7286SNP arrayGenotyping20
nssv15684894copy number lossOCD15-B_MN-1465SNP arrayGenotyping20
nssv15685250copy number lossOCD1163-0625-7948-3SNP arrayGenotyping26
nssv15685467copy number lossOCD12-S_896223SNP arrayGenotyping21
nssv15686316copy number lossOCD31-S_896572SNP arrayGenotyping28
nssv15686339copy number lossOCD129-8961043SNP arrayGenotyping22
nssv15686670copy number lossOCD16-B_CW-1426SNP arrayGenotyping21
nssv15686856copy number lossOCD29-B_JL-1243SNP arrayGenotyping19
nssv15688121copy number loss209355SNP arrayGenotyping28
nssv15690808copy number lossOCD17-S_896321SNP arrayGenotyping22
nssv15691240copy number lossOCD29-B_OL-1241SNP arrayGenotyping20
nssv15691413copy number lossOCD42-S_0625-2765-2SNP arrayGenotyping25
nssv15692307copy number lossOCD55-0625-9391-1SNP arrayGenotyping23
nssv15692764copy number lossOCD72-896553SNP arrayGenotyping17
nssv15693583copy number lossOCD94-JW-267SNP arrayGenotyping15
nssv15697169copy number loss155474SNP arrayGenotyping16
nssv15697960copy number loss216470SNP arrayGenotyping20
nssv15700418copy number loss206133SNP arrayGenotyping18

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15618924RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15619038RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15627383RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15628515RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15630764RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15633287RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15641191RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15644673RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15646536RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15653120RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15658971RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15660544RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15660604RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15664084RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15670263RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15671500RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15672725RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15674838RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15676373RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15682633RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15682747RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15684204RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15684311RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15684894RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15685250RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15685467RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15686316RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15686339RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15686670RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15686856RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15688121RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15690808RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15691240RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15691413RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15692307RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15692764RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15693583RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15697169RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15697960RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15700418RemappedPerfectNC_000010.11:g.(?_
50070587)_(5014399
6_?)del
GRCh38.p12First PassNC_000010.11Chr1050,070,58750,143,996
nssv15618924Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15619038Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15627383Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15628515Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15630764Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15633287Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15641191Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15644673Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15646536Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15653120Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15658971Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15660544Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15660604Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15664084Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15670263Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15671500Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15672725Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15674838Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15676373Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15682633Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15682747Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15684204Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15684311Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15684894Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15685250Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15685467Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15686316Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15686339Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15686670Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15686856Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15688121Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15690808Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15691240Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15691413Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15692307Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15692764Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15693583Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15697169Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15697960Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756
nssv15700418Submitted genomicNC_000010.10:g.(?_
51830347)_(5190375
6_?)del
GRCh37 (hg19)NC_000010.10Chr1051,830,34751,903,756

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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