A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723359



Internal ID147025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39824656..39824792hg38UCSC Ensembl
chr19:40315296..40315432hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723359
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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