A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935069



Internal ID22710405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27762103..27762311hg38UCSC Ensembl
chr19:28253011..28253219hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935069
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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