A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654651



Internal ID15391303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43276976..43277636hg38UCSC Ensembl
Innerchr6:43244714..43245374hg19UCSC Ensembl
Innerchr6:43352692..43353352hg18UCSC Ensembl
Innerchr6:43352692..43353352hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
hg17661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517442
Supporting Variants
Samples
Known GenesTTBK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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