A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732337



Internal ID156003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38949893..39066919hg38UCSC Ensembl
chr20:37578536..37695562hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38117027
hg19117027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513925
Supporting Variants
Samples
Known GenesDHX35, FAM83D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732337
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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