A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522018



Internal ID21846377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233722831..233725340hg38UCSC Ensembl
chr2:234631477..234633986hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg382510
hg192510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987972
Supporting Variants
Samples
Known GenesUGT1A10, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522018
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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