A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1085464



Internal ID15938650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63922745..64387516hg38UCSC Ensembl
Innerchr7:63383123..63847894hg19UCSC Ensembl
Innerchr7:63020558..63485329hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38464772
hg19464772
hg18464772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607304
Supporting Variants
Samples
Known GenesLINC01005, ZNF679, ZNF727, ZNF735, ZNF736
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1085464
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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