A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044969



Internal ID21954239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54072847..54072908hg38UCSC Ensembl
chr20:52689386..52689447hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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