A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590443



Internal ID16031166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62664449..62675160hg38UCSC Ensembl
Innerchr3:62650124..62660835hg19UCSC Ensembl
Innerchr3:62625164..62635875hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3810712
hg1910712
hg1810712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151907
SamplesHGDP01182
Known GenesCADPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590443
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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