A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591864



Internal ID16379273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140611266..140731813hg38UCSC Ensembl
Innerchr3:140330108..140450655hg19UCSC Ensembl
Innerchr3:141812798..141933345hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38120548
hg19120548
hg18120548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152544
Samples1780862001_A
Known GenesTRIM42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591864
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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