A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633548



Internal ID21825595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48935988..48936162hg38UCSC Ensembl
chr20:47552525..47552699hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045802
Supporting Variants
Samples
Known GenesARFGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633548
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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