A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685112



Internal ID15421764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6613344..6620173hg38UCSC Ensembl
Innerchr10:6655306..6662135hg19UCSC Ensembl
Innerchr10:6695312..6702141hg18UCSC Ensembl
Innerchr10:6695312..6702141hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386830
hg196830
hg186830
hg176830
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517486
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685112
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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