A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084678



Internal ID15937864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54642285..54659616hg38UCSC Ensembl
Innerchr7:54709978..54727309hg19UCSC Ensembl
Innerchr7:54677472..54694803hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3817332
hg1917332
hg1817332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084678
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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