A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945776



Internal ID22721257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33617465..33623322hg38UCSC Ensembl
chr19:34108371..34114228hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg385858
hg195858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392560
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945776
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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