A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519335



Internal ID15446628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38802156..38805661hg38UCSC Ensembl
Innerchr3:38843647..38847152hg19UCSC Ensembl
Innerchr3:38818651..38822156hg18UCSC Ensembl
Innerchr3:38818651..38822156hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg383506
hg193506
hg183506
hg173506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655477, nssv693193
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519335
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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