A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524442



Internal ID15451735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54880600..54947298hg38UCSC Ensembl
Innerchr20:53497139..53563837hg19UCSC Ensembl
Innerchr20:52930546..52997244hg18UCSC Ensembl
Innerchr20:52930546..52997244hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3866699
hg1966699
hg1866699
hg1766699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv248n21
Supporting Variantsnssv700374
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524442
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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