A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582876



Internal ID16370285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:123017084..123047550hg38UCSC Ensembl
Innerchr2:123774660..123805126hg19UCSC Ensembl
Innerchr2:123491130..123521596hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3830467
hg1930467
hg1830467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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