A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584796



Internal ID16372205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239684069..239741119hg38UCSC Ensembl
Innerchr2:240605763..240662813hg19UCSC Ensembl
Innerchr2:240270700..240327750hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3857051
hg1957051
hg1857051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151183
Samples1780862197_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584796
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