A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592144



Internal ID16379553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162081302..162376642hg38UCSC Ensembl
Innerchr3:161799090..162094430hg19UCSC Ensembl
Innerchr3:163281784..163577124hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38295341
hg19295341
hg18295341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151817
SamplesHGDP01336
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592144
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