A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941623



Internal ID22717050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35917846..35929271hg38UCSC Ensembl
chr19:36408748..36420173hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811426
hg1911426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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