A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155213



Internal ID15529525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79690614..79765565hg38UCSC Ensembl
Innerchr7:79319930..79394881hg19UCSC Ensembl
Innerchr7:79157866..79232817hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3874952
hg1974952
hg1874952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607674
Supporting Variants
SamplesHGDP00801
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155213
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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