A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590442



Internal ID16031165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62624950..62626338hg38UCSC Ensembl
Innerchr3:62610625..62612013hg19UCSC Ensembl
Innerchr3:62585665..62587053hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381389
hg191389
hg181389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151905, nssv1151906, nssv1151904
SamplesHGDP01255, HGDP00908, HGDP01088
Known GenesCADPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590442
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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