A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945679



Internal ID22721159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55399019..55399197hg38UCSC Ensembl
chr19:55910387..55910565hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945679
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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