A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542477



Internal ID21866832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113667118..113667118hg38UCSC Ensembl
chr3:113385965..113385965hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076045
Supporting Variants
Samples
Known GenesKIAA2018
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542477
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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