A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724436



Internal ID148102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58260316..58270394hg38UCSC Ensembl
chr19:58771682..58781760hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3810079
hg1910079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527100
Supporting Variants
Samples
Known GenesZNF544
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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