A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189959



Internal ID20756999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35943601..35945300hg38UCSC Ensembl
chr11:35965151..35966850hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458489
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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