A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559758



Internal ID21884113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181226410..181226410hg38UCSC Ensembl
chr5:180653410..180653410hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382585
hg192585
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063115
Supporting Variants
Samples
Known GenesTRIM41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559758
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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