A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532291



Internal ID308217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56087868..56087959hg38UCSC Ensembl
chr19:56599234..56599325hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725751
Samples
Known GenesZNF787
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532291
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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