A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183780



Internal ID20750820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117390103..117479809hg38UCSC Ensembl
chr11:117260819..117350524hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3889707
hg1989706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466411
Supporting Variants
Samples
Known GenesCEP164, DSCAML1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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