A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520675



Internal ID296994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11561448..11571075hg38UCSC Ensembl
chr19:11672263..11681890hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389628
hg199628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520675
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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