A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523886



Internal ID15451179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5847729..5859893hg38UCSC Ensembl
Innerchr20:5828375..5840539hg19UCSC Ensembl
Innerchr20:5776375..5788539hg18UCSC Ensembl
Innerchr20:5776375..5788539hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3812165
hg1912165
hg1812165
hg1712165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699728
Samples
Known GenesC20orf196
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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