A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182099



Internal ID20749139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11122588..11150333hg38UCSC Ensembl
chr18:11122587..11150332hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3827746
hg1927746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522647
Supporting Variants
Samples
Known GenesPIEZO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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