A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582119



Internal ID16022842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61448544..61594736hg38UCSC Ensembl
Innerchr2:61675679..61821871hg19UCSC Ensembl
Innerchr2:61529183..61675375hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38146193
hg19146193
hg18146193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911333
Samples
Known GenesUSP34, XPO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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