A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395080



Internal ID22452950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13693672..13695403hg38UCSC Ensembl
chr19:13804486..13806217hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381732
hg191732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395080
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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