A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193845



Internal ID20760885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80691835..80758963hg38UCSC Ensembl
chr11:80402879..80470006hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3867129
hg1967128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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