A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368211



Internal ID22593880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106433886..106436363hg38UCSC Ensembl
chr13:107086234..107088711hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368211
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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