A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690083



Internal ID15080049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31489801hg38UCSC Ensembl
Innerchr6:31360389..31457578hg19UCSC Ensembl
Innerchr6:31468368..31565557hg18UCSC Ensembl
Innerchr6:31468368..31565557hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3897190
hg1997190
hg1897190
hg1797190
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690083
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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