A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683682



Internal ID15420334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11437771..11442946hg38UCSC Ensembl
Innerchr10:11479770..11484945hg19UCSC Ensembl
Innerchr10:11519776..11524951hg18UCSC Ensembl
Innerchr10:11519776..11524951hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385176
hg195176
hg185176
hg175176
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515865
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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