A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655790



Internal ID18607385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31385552..31497326hg38UCSC Ensembl
Innerchr6:31353329..31465103hg19UCSC Ensembl
Innerchr6:31461308..31573082hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38111775
hg19111775
hg18111775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034727
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)nssv3655790
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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