A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693165



Internal ID116831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73325331..73325369hg38UCSC Ensembl
chr13:73899468..73899506hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693165
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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