A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526467



Internal ID15453760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14049928..14082406hg38UCSC Ensembl
Innerchr3:14091428..14123906hg19UCSC Ensembl
Innerchr3:14066429..14098907hg18UCSC Ensembl
Innerchr3:14066429..14098907hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3832479
hg1932479
hg1832479
hg1732479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702771
Samples
Known GenesTPRXL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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