A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723164



Internal ID146830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37208029..37208085hg38UCSC Ensembl
chr19:37698931..37698987hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520158
Supporting Variants
Samples
Known GenesZNF585B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723164
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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