A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272720



Internal ID20481938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59298588..59298588hg38UCSC Ensembl
chr18:56965820..56965820hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762590
Supporting Variants
Samples
Known GenesCPLX4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272720
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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