A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048982



Internal ID21958216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63339961..63340372hg38UCSC Ensembl
chr20:61971313..61971724hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048982
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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