A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521788



Internal ID20895149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8250384..8250957hg38UCSC Ensembl
chr20:8231031..8231604hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070553
Samples
Known GenesPLCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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