A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681446



Internal ID15418098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129581448..129598742hg38UCSC Ensembl
Innerchr3:129300291..129317585hg19UCSC Ensembl
Innerchr3:130782981..130800275hg18UCSC Ensembl
Innerchr3:130782989..130800283hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3817295
hg1917295
hg1817295
hg1717295
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)nssv681446
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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