A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515892



Internal ID15096499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9156777..9171449hg38UCSC Ensembl
Innerchr20:9137424..9152096hg19UCSC Ensembl
Innerchr20:9085424..9100096hg18UCSC Ensembl
Innerchr20:9085424..9100096hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3814673
hg1914673
hg1814673
hg1714673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692836, nssv665175
Samples
Known GenesPLCB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515892
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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