A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705755



Internal ID15095721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9329066..9336619hg38UCSC Ensembl
Innerchr20:9309713..9317266hg19UCSC Ensembl
Innerchr20:9257713..9265266hg18UCSC Ensembl
Innerchr20:9257713..9265266hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg387554
hg197554
hg187554
hg177554
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529042
Supporting Variants
Samples
Known GenesPLCB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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