A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723057



Internal ID146723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36018042..36084494hg38UCSC Ensembl
chr19:36508944..36575396hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3866453
hg1966453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528024
Supporting Variants
Samples
Known GenesCLIP3, THAP8, WDR62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723057
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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