A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526796



Internal ID15107403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35556975..35582252hg38UCSC Ensembl
Innerchr20:34144746..34170174hg19UCSC Ensembl
Innerchr20:33608160..33633588hg18UCSC Ensembl
Innerchr20:33608160..33633588hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3825278
hg1925429
hg1825429
hg1725429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703150
Samples
Known GenesERGIC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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