A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528762



Internal ID304806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21551644..21551731hg38UCSC Ensembl
chr19:21734446..21734533hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528762
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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