A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939798



Internal ID22715196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19732377..19922535hg38UCSC Ensembl
chr19:19843186..20033344hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38190159
hg19190159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396957
Samples
Known GenesLINC00663, ZNF14, ZNF253, ZNF506, ZNF93
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939798
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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