A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591963



Internal ID16379372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146929517..147189411hg38UCSC Ensembl
Innerchr3:146647304..146907198hg19UCSC Ensembl
Innerchr3:148129994..148389888hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38259895
hg19259895
hg18259895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976375
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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