A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520828



Internal ID15101435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129570909..129645354hg38UCSC Ensembl
Innerchr3:129289752..129364197hg19UCSC Ensembl
Innerchr3:130772442..130846887hg18UCSC Ensembl
Innerchr3:130772450..130846895hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3874446
hg1974446
hg1874446
hg1774446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697637
Samples
Known GenesPLXND1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520828
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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