A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941029



Internal ID22716446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44073695..44082218hg38UCSC Ensembl
chr19:44577848..44586371hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg388524
hg198524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394941
Samples
Known GenesZNF284
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941029
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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