A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697632



Internal ID15434284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108399337..108433619hg38UCSC Ensembl
Innerchr10:110159095..110193377hg19UCSC Ensembl
Innerchr10:110149085..110183367hg18UCSC Ensembl
Innerchr10:110149085..110183367hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3834283
hg1934283
hg1834283
hg1734283
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520820
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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