A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731934



Internal ID155600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32061000..32066100hg38UCSC Ensembl
chr20:30648803..30653903hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518232
Supporting Variants
Samples
Known GenesHCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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