A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721746



Internal ID145412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15119948..15119955hg38UCSC Ensembl
chr19:15230759..15230766hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552715
Supporting Variants
Samples
Known GenesILVBL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721746
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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