A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582058



Internal ID16369467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56665450..56789257hg38UCSC Ensembl
Innerchr2:56892585..57016392hg19UCSC Ensembl
Innerchr2:56746089..56869896hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38123808
hg19123808
hg18123808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911181
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582058
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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