A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692331



Internal ID115997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106661420..106661433hg38UCSC Ensembl
chr13:107313768..107313781hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557127
Supporting Variants
Samples
Known GenesLINC00443
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692331
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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