A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566900



Internal ID21758943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168755389..168755449hg38UCSC Ensembl
chr5:168182394..168182454hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009893
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566900
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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