A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183084



Internal ID20750124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25065071..25104797hg38UCSC Ensembl
chr11:25086617..25126343hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3839727
hg1939727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436218
Supporting Variants
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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