A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732270



Internal ID155936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37607045..37607778hg38UCSC Ensembl
chr20:36235447..36236180hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732270
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer