A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723059



Internal ID146725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36029513..36044516hg38UCSC Ensembl
chr19:36520415..36535418hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3815004
hg1915004
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531520
Supporting Variants
Samples
Known GenesCLIP3, THAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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