A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602632



Internal ID21794679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99301527..99301527hg38UCSC Ensembl
chr13:99953781..99953781hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085700
Supporting Variants
Samples
Known GenesGPR183, MIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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