A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526233



Internal ID15453526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58622882..58628992hg38UCSC Ensembl
Innerchr20:57197938..57204048hg19UCSC Ensembl
Innerchr20:56631344..56637454hg18UCSC Ensembl
Innerchr20:56631344..56637454hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg386111
hg196111
hg186111
hg176111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702500
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526233
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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