A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526083



Internal ID15453376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5448343..5507202hg38UCSC Ensembl
Innerchr20:5428989..5487848hg19UCSC Ensembl
Innerchr20:5376989..5435848hg18UCSC Ensembl
Innerchr20:5376989..5435848hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3858860
hg1958860
hg1858860
hg1758860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702327
Samples
Known GenesLINC00654, LOC643406
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526083
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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