A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519672



Internal ID15100279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100359197..100372778hg38UCSC Ensembl
Innerchr10:102118954..102132535hg19UCSC Ensembl
Innerchr10:102108944..102122525hg18UCSC Ensembl
Innerchr10:102108944..102122525hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3813582
hg1913582
hg1813582
hg1713582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694341
Samples
Known GenesSCD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519672
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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