A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929979



Internal ID22705239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45566180..45566501hg38UCSC Ensembl
chr19:46069438..46069759hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396298
Samples
Known GenesOPA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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