A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583499



Internal ID16024222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:161162132..161270523hg38UCSC Ensembl
Innerchr2:162018643..162127034hg19UCSC Ensembl
Innerchr2:161726889..161835280hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38108392
hg19108392
hg18108392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7140n54
Supporting Variantsnssv923515
Samples
Known GenesTANK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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