A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519565



Internal ID295914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13998336..14000268hg38UCSC Ensembl
chr19:14109148..14111080hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721643
Samples
Known GenesRFX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519565
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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