A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681345



Internal ID15071311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33087761..33118074hg38UCSC Ensembl
Innerchr6:33055538..33085851hg19UCSC Ensembl
Innerchr6:33163516..33193829hg18UCSC Ensembl
Innerchr6:33163516..33193829hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3830314
hg1930314
hg1830314
hg1730314
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516221
Supporting Variants
Samples
Known GenesHLA-DPB1, HLA-DPB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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