A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046763



Internal ID21955996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32176506..32177172hg38UCSC Ensembl
chr20:30764309..30764975hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046763
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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