A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150749



Internal ID15873963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228501467..228566625hg38UCSC Ensembl
Innerchr2:229366183..229431341hg19UCSC Ensembl
Innerchr2:229074427..229139585hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3865159
hg1965159
hg1865159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584630
Supporting Variants
SamplesHGDP00451
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150749
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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