A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522920



Internal ID15103527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17832478..17854507hg38UCSC Ensembl
Innerchr21:19204795..19226824hg19UCSC Ensembl
Innerchr21:18126666..18148695hg18UCSC Ensembl
Innerchr21:18126666..18148695hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3822030
hg1922030
hg1822030
hg1722030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698581
Samples
Known GenesCHODL-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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