A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733252



Internal ID156918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56712899..56713164hg38UCSC Ensembl
chr20:55287955..55288220hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733252
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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