A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721099



Internal ID144765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8061732..8061732hg38UCSC Ensembl
chr19:8126616..8126616hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535252
Supporting Variants
Samples
Known GenesCCL25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721099
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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