A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522204



Internal ID15102811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43800602..43826445hg38UCSC Ensembl
Innerchr21:45220483..45246326hg19UCSC Ensembl
Innerchr21:44044911..44070754hg18UCSC Ensembl
Innerchr21:44044911..44070754hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3825844
hg1925844
hg1825844
hg1725844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694977
Samples
Known GenesLOC284837, RRP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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