A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581156



Internal ID16368565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20146551..20157183hg38UCSC Ensembl
Innerchr2:20346312..20356944hg19UCSC Ensembl
Innerchr2:20209793..20220425hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3810633
hg1910633
hg1810633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904415
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer