A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725771



Internal ID149437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56222010..56247045hg38UCSC Ensembl
chr19:56733379..56758414hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3825036
hg1925036
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563731
Supporting Variants
Samples
Known GenesZSCAN5A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725771
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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