A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532681



Internal ID308596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9752902..9761161hg38UCSC Ensembl
chr19:9863578..9871837hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388260
hg198260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721251
Samples
Known GenesZNF846
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532681
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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