A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731940



Internal ID155606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32176556..32177600hg38UCSC Ensembl
chr20:30764359..30765403hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731940
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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