A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929398



Internal ID22704651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52683434..52978645hg38UCSC Ensembl
chr19:53186687..53481898hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38295212
hg19295212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1073n209
Supporting Variantsnssv17397084
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929398
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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