A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732358



Internal ID156024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39464923..39465175hg38UCSC Ensembl
chr20:38093566..38093818hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732358
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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