A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982282



Internal ID21891625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205957905..205958414hg38UCSC Ensembl
chr17:4174726..4175192hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38510
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537440
Samples
Known GenesUBE2G1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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