A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582009



Internal ID16022732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53474186..53557900hg38UCSC Ensembl
Innerchr2:53701324..53785037hg19UCSC Ensembl
Innerchr2:53554828..53638541hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3883715
hg1983714
hg1883714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150724
Samples1798860279_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582009
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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