A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392560



Internal ID22450430
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 StatusS
Merged Variantsnsv5945776
Supporting Variants
Samples
Known GenesCHST8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392560
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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