A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047076



Internal ID21956309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37572180..37572418hg38UCSC Ensembl
chr20:36200582..36200820hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047076
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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