A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056502



Internal ID21965735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5582205..5583072hg38UCSC Ensembl
chr20:5562851..5563718hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635939
Samples
Known GenesGPCPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056502
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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