A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725919



Internal ID149585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35337773..35338583hg38UCSC Ensembl
chr20:33925576..33926386hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514727
Supporting Variants
Samples
Known GenesUQCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725919
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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