A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590051



Internal ID16377460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33468269..33561415hg38UCSC Ensembl
Innerchr3:33509761..33602907hg19UCSC Ensembl
Innerchr3:33484765..33577911hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3893147
hg1993147
hg1893147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152230
SamplesHGDP01010
Known GenesCLASP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590051
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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