A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516266



Internal ID292729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41457246..41457329hg38UCSC Ensembl
chr19:41963151..41963235hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3884
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723502
Samples
Known GenesLOC100505495
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516266
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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