A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662123



Internal ID18960404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122203647..122289544hg38UCSC Ensembl
Innerchr7:121843701..121929598hg19UCSC Ensembl
Innerchr7:121630937..121716834hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3885898
hg1985898
hg1885898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020645
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)nssv3662123
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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