A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520518



Internal ID15447811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144568113..144591901hg38UCSC Ensembl
Innerchr4:145489265..145513053hg19UCSC Ensembl
Innerchr4:145708715..145732503hg18UCSC Ensembl
Innerchr4:145846870..145870658hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3823789
hg1923789
hg1823789
hg1723789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697465
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520518
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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