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nsv4375217

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,220

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 478 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):156,044,674-156,082,893Question Mark
Overlapping variant regions from other studies: 478 SVs from 73 studies. See in: genome view    
Submitted genomic155,471,684-155,509,903Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4375217RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5156,044,674156,082,893
nsv4375217Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5155,471,684155,509,903

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15613709copy number loss1-0718-003SNP arrayGenotyping35
nssv15667754copy number loss7-0059-003SNP arrayGenotyping18

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15613709RemappedPerfectNC_000005.10:g.(?_
156044674)_(156082
893_?)del
GRCh38.p12First PassNC_000005.10Chr5156,044,674156,082,893
nssv15667754RemappedPerfectNC_000005.10:g.(?_
156044674)_(156082
893_?)del
GRCh38.p12First PassNC_000005.10Chr5156,044,674156,082,893
nssv15613709Submitted genomicNC_000005.9:g.(?_1
55471684)_(1555099
03_?)del
GRCh37 (hg19)NC_000005.9Chr5155,471,684155,509,903
nssv15667754Submitted genomicNC_000005.9:g.(?_1
55471684)_(1555099
03_?)del
GRCh37 (hg19)NC_000005.9Chr5155,471,684155,509,903

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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