A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591854



Internal ID16032577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138629239..139045387hg38UCSC Ensembl
Innerchr3:138348081..138764229hg19UCSC Ensembl
Innerchr3:139830771..140246919hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38416149
hg19416149
hg18416149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974770
Samples
Known GenesC3orf72, FAIM, FOXL2, PIK3CB, PRR23A, PRR23B, PRR23C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591854
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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