A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723585



Internal ID147251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45519452..45519762hg38UCSC Ensembl
chr19:46022710..46023020hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538036
Supporting Variants
Samples
Known GenesVASP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723585
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03935


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