A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521548



Internal ID297841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23369034..23369116hg38UCSC Ensembl
chr19:23551836..23551918hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725041
Samples
Known GenesZNF91
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521548
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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