A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697650



Internal ID15087616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10671531..10724327hg38UCSC Ensembl
Innerchr6:10671764..10724560hg19UCSC Ensembl
Innerchr6:10779750..10832546hg18UCSC Ensembl
Innerchr6:10779750..10832546hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3852797
hg1952797
hg1852797
hg1752797
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520853
Supporting Variants
Samples
Known GenesC6orf52, PAK1IP1, TMEM14C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697650
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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