A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582097



Internal ID16369506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:58038964..58119831hg38UCSC Ensembl
Innerchr2:58266099..58346966hg19UCSC Ensembl
Innerchr2:58119603..58200470hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3880868
hg1980868
hg1880868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911271
Samples
Known GenesVRK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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