A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695518



Internal ID15432170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108758303..108759061hg38UCSC Ensembl
Innerchr6:109079506..109080264hg19UCSC Ensembl
Innerchr6:109186199..109186957hg18UCSC Ensembl
Innerchr6:109186199..109186957hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38759
hg19759
hg18759
hg17759
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518105
Supporting Variants
Samples
Known GenesLINC00222
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695518
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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