A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178358



Internal ID20745398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18707713..18708501hg38UCSC Ensembl
chr11:18729260..18730048hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447251
Supporting Variants
Samples
Known GenesIGSF22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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