A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182967



Internal ID20750007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68336508..68339387hg38UCSC Ensembl
chr11:68103976..68106855hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382880
hg192880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470395
Supporting Variants
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182967
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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