A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598558



Internal ID21790603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58996219..58996219hg38UCSC Ensembl
chr15:59288418..59288418hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094183
Supporting Variants
Samples
Known GenesRNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598558
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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