A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655865



Internal ID18607460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392318..31498018hg38UCSC Ensembl
Innerchr6:31360095..31465795hg19UCSC Ensembl
Innerchr6:31468074..31573774hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38105701
hg19105701
hg18105701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030071
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655865
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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