A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581870



Internal ID16369279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51080937..51252032hg38UCSC Ensembl
Innerchr2:51308075..51479170hg19UCSC Ensembl
Innerchr2:51161579..51332674hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38171096
hg19171096
hg18171096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6867n54
Supporting Variantsnssv908398
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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