A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608891



Internal ID21800938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106520974..106522405hg38UCSC Ensembl
chr13:107173322..107174753hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381432
hg191432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021497
Supporting Variants
Samples
Known GenesEFNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608891
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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