A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933098



Internal ID22708406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44161233..44161363hg38UCSC Ensembl
chr19:44665386..44665516hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933098
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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