A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581929



Internal ID16369338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52372222..52534101hg38UCSC Ensembl
Innerchr2:52599360..52761239hg19UCSC Ensembl
Innerchr2:52452864..52614743hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38161880
hg19161880
hg18161880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908718
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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