A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610873



Internal ID21802920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68221886..68221886hg38UCSC Ensembl
chr15:68514224..68514224hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092203
Supporting Variants
Samples
Known GenesCLN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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