A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv925266



Internal ID16219222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:166701394..166733235hg38UCSC Ensembl
Innerchr2:167557904..167589745hg19UCSC Ensembl
Innerchr2:167266150..167297991hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3831842
hg1931842
hg1831842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583588
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv925266
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