A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049872



Internal ID21959105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35600890..35602511hg38UCSC Ensembl
chr20:34188812..34190433hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049872
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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