A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761250



Internal ID16055206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131042127..131058568hg38UCSC Ensembl
Innerchr10:132840390..132856831hg19UCSC Ensembl
Innerchr10:132730380..132746821hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816442
hg1916442
hg1816442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552388
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761250
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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