A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589721



Internal ID16377130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12949883..13025035hg38UCSC Ensembl
Innerchr3:12991383..13066535hg19UCSC Ensembl
Innerchr3:12966383..13041535hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3875153
hg1975153
hg1875153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959133
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589721
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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