A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581200



Internal ID16368609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24491661..24496248hg38UCSC Ensembl
Innerchr2:24714530..24719117hg19UCSC Ensembl
Innerchr2:24568034..24572621hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384588
hg194588
hg184588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904510
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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