A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604028



Internal ID21796075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75554078..75555941hg38UCSC Ensembl
chr13:76128214..76130077hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026466
Supporting Variants
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604028
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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