A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583438



Internal ID16370847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156793445..156854701hg38UCSC Ensembl
Innerchr2:157649957..157711213hg19UCSC Ensembl
Innerchr2:157358203..157419459hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3861257
hg1961257
hg1861257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv922155
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583438
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