A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662204



Internal ID18960485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131763957..131775023hg38UCSC Ensembl
Innerchr7:131448716..131459782hg19UCSC Ensembl
Innerchr7:131099256..131110322hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3811067
hg1911067
hg1811067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019918
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662204
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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