A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680983



Internal ID15070949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33087761..33093172hg38UCSC Ensembl
Innerchr6:33055538..33060949hg19UCSC Ensembl
Innerchr6:33163516..33168927hg18UCSC Ensembl
Innerchr6:33163516..33168927hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385412
hg195412
hg185412
hg175412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516221
Supporting Variants
Samples
Known GenesHLA-DPB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680983
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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