A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986153



Internal ID21895496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137331015..137331252hg38UCSC Ensembl
chr2:138088585..138088822hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528319
Samples
Known GenesTHSD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986153
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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