A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023918



Internal ID21933261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106518412..106520968hg38UCSC Ensembl
chr13:107170760..107173316hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg382557
hg192557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601368
Samples
Known GenesEFNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023918
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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