A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590444



Internal ID16031167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62721844..62728634hg38UCSC Ensembl
Innerchr3:62707519..62714309hg19UCSC Ensembl
Innerchr3:62682559..62689349hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg386791
hg196791
hg186791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151908
SamplesHGDP00932
Known GenesCADPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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