A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684218



Internal ID15074184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31386783..31483699hg38UCSC Ensembl
Innerchr6:31354560..31451476hg19UCSC Ensembl
Innerchr6:31462539..31559455hg18UCSC Ensembl
Innerchr6:31462539..31559455hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3896917
hg1996917
hg1896917
hg1796917
Variant TypeCNV gain
Copy Number
Allele State
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)nssv684218
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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