A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041687



Internal ID21951018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50632086..50632810hg38UCSC Ensembl
chr20:49248623..49249347hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622928
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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