A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693803



Internal ID117469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113148390..113148441hg38UCSC Ensembl
chr13:113802704..113802755hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550994
Supporting Variants
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693803
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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