A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529789



Internal ID305795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57690157..57699388hg38UCSC Ensembl
chr19:58201525..58210756hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg389232
hg199232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529789
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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