A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686972



Internal ID15423624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3749032..3750546hg38UCSC Ensembl
Innerchr10:3791224..3792738hg19UCSC Ensembl
Innerchr10:3781224..3782738hg18UCSC Ensembl
Innerchr10:3781224..3782738hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg381515
hg191515
hg181515
hg171515
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517787
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686972
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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