A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521514



Internal ID15448807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146929517..147189411hg38UCSC Ensembl
Innerchr3:146647304..146907198hg19UCSC Ensembl
Innerchr3:148129994..148389888hg18UCSC Ensembl
Innerchr3:148130002..148389896hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38259895
hg19259895
hg18259895
hg17259895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698131
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521514
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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