A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933474



Internal ID22708787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9752902..9761160hg38UCSC Ensembl
chr19:9863578..9871836hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388259
hg198259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397152
Samples
Known GenesZNF846
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933474
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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