A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581199



Internal ID16368608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24491453..24491661hg38UCSC Ensembl
Innerchr2:24714322..24714530hg19UCSC Ensembl
Innerchr2:24567826..24568034hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38209
hg19209
hg18209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904509
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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