A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625347



Internal ID21817394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48935660..48936010hg38UCSC Ensembl
chr20:47552197..47552547hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043667
Supporting Variants
Samples
Known GenesARFGEF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625347
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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