A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695882



Internal ID15432534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29376927..29378552hg38UCSC Ensembl
Innerchr6:29344704..29346329hg19UCSC Ensembl
Innerchr6:29452683..29454308hg18UCSC Ensembl
Innerchr6:29452683..29454308hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381626
hg191626
hg181626
hg171626
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519453
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695882
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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