A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614890



Internal ID21806937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111972545..111975848hg38UCSC Ensembl
chr13:112626859..112630162hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614890
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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