A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150707



Internal ID15874897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5308496..5360169hg38UCSC Ensembl
Innerchr2:5448629..5500302hg19UCSC Ensembl
Innerchr2:5366080..5417753hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3851674
hg1951674
hg1851674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580865
Supporting Variants
SamplesHGDP00607
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150707
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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