A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655863



Internal ID15392515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129581448..129615390hg38UCSC Ensembl
Innerchr3:129300291..129334233hg19UCSC Ensembl
Innerchr3:130782981..130816923hg18UCSC Ensembl
Innerchr3:130782989..130816931hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3833943
hg1933943
hg1833943
hg1733943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519392
Supporting Variants
Samples
Known GenesPLXND1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655863
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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