A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723056



Internal ID146722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36016874..36114874hg38UCSC Ensembl
chr19:36507776..36605776hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3898001
hg1998001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145427
Supporting Variants
Samples
Known GenesCLIP3, OVOL3, POLR2I, THAP8, WDR62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723056
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001684


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