A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526269



Internal ID302405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16693750..16706452hg38UCSC Ensembl
chr19:16804561..16817263hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3812703
hg1912703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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