A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091899



Internal ID15945085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101527747hg38UCSC Ensembl
Innerchr7:100968363..101171028hg19UCSC Ensembl
Innerchr7:100755083..100957748hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38202666
hg19202666
hg18202666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607981
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091899
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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