A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582096



Internal ID16369505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57968975..58010589hg38UCSC Ensembl
Innerchr2:58196110..58237724hg19UCSC Ensembl
Innerchr2:58049614..58091228hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3841615
hg1941615
hg1841615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150461
SamplesHGDP00611
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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