A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044654



Internal ID21953936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63630444..63634130hg38UCSC Ensembl
chr20:62261797..62265483hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383687
hg193687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044654
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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