A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519392



Internal ID15446685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129581448..129645354hg38UCSC Ensembl
Innerchr3:129300291..129364197hg19UCSC Ensembl
Innerchr3:130782981..130846887hg18UCSC Ensembl
Innerchr3:130782989..130846895hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3863907
hg1963907
hg1863907
hg1763907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682380, nssv655863, nssv681446
Samples
Known GenesPLXND1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519392
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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