A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581335



Internal ID16368744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33836277..33938347hg38UCSC Ensembl
Innerchr2:34061344..34163414hg19UCSC Ensembl
Innerchr2:33914848..34016918hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38102071
hg19102071
hg18102071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6757n54
Supporting Variantsnssv1150208
SamplesHGDP00557
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581335
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