A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722897



Internal ID146563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33719676..33744473hg38UCSC Ensembl
chr19:34210581..34235378hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3824798
hg1924798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525425
Supporting Variants
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722897
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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