A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519101



Internal ID295457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34452668..34452740hg38UCSC Ensembl
chr20:33040473..33040545hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732100
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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