A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755411



Internal ID19053692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79928695..79995770hg38UCSC Ensembl
Innerchr7:79558011..79625086hg19UCSC Ensembl
Innerchr7:79395947..79463022hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3867076
hg1967076
hg1867076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032480
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)nssv3755411
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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