A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581797



Internal ID16369206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49287592..49327844hg38UCSC Ensembl
Innerchr2:49514731..49554983hg19UCSC Ensembl
Innerchr2:49368235..49408487hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3840253
hg1940253
hg1840253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6856n54
Supporting Variantsnssv908244
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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