A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518703



Internal ID295074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35974592..35977180hg38UCSC Ensembl
chr19:36465494..36468082hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382589
hg192589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518703
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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