A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598698



Internal ID21790743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68221824..68221824hg38UCSC Ensembl
chr15:68514162..68514162hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086542
Supporting Variants
Samples
Known GenesCLN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598698
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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