A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521490



Internal ID15448783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127013316..127065146hg38UCSC Ensembl
Innerchr3:126732159..126783989hg19UCSC Ensembl
Innerchr3:128214849..128266679hg18UCSC Ensembl
Innerchr3:128214857..128266687hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3851831
hg1951831
hg1851831
hg1751831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694453
Samples
Known GenesPLXNA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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