A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724353



Internal ID148019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57545295..57545716hg38UCSC Ensembl
chr19:58056663..58057084hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518503
Supporting Variants
Samples
Known GenesZNF550
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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