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nsv4382988

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52,281

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 514 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):56,195,132-56,247,412Question Mark
Overlapping variant regions from other studies: 514 SVs from 72 studies. See in: genome view    
Submitted genomic56,706,501-56,758,781Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4382988RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1956,195,13256,247,412
nsv4382988Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1956,706,50156,758,781

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15651722copy number gain2-1547-003SNP arrayGenotyping13

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15651722RemappedPerfectNC_000019.10:g.(?_
56195132)_(5624741
2_?)dup
GRCh38.p12First PassNC_000019.10Chr1956,195,13256,247,412
nssv15651722Submitted genomicNC_000019.9:g.(?_5
6706501)_(56758781
_?)dup
GRCh37 (hg19)NC_000019.9Chr1956,706,50156,758,781

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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