A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941957



Internal ID22717388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58349383..58363852hg38UCSC Ensembl
chr19:58860749..58875219hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3814470
hg1914471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392675
Samples
Known GenesA1BG, A1BG-AS1, ZNF497
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941957
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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