A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150791



Internal ID15853505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:181110525..181175566hg38UCSC Ensembl
Innerchr2:181975252..182040293hg19UCSC Ensembl
Innerchr2:181683497..181748538hg18UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3865042
hg1965042
hg1865042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583910
Supporting Variants
Samples1780854238_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150791
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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