A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528402



Internal ID15109009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9171449..9175556hg38UCSC Ensembl
Innerchr20:9152096..9156203hg19UCSC Ensembl
Innerchr20:9100096..9104203hg18UCSC Ensembl
Innerchr20:9100096..9104203hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384108
hg194108
hg184108
hg174108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704992
Samples
Known GenesPLCB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528402
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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