A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591971



Internal ID16032694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:148010995..148149841hg38UCSC Ensembl
Innerchr3:147728782..147867628hg19UCSC Ensembl
Innerchr3:149211472..149350318hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38138847
hg19138847
hg18138847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976382
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591971
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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