A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194192



Internal ID20761232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73744879..73754845hg38UCSC Ensembl
chr11:73455924..73465890hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg389967
hg199967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455912
Supporting Variants
Samples
Known GenesRAB6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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