A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558294



Internal ID21882649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168736684..168736684hg38UCSC Ensembl
chr5:168163689..168163689hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079941
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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