A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194362



Internal ID20761402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134671383..134868514hg38UCSC Ensembl
chr11:134541277..134738408hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38197132
hg19197132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458260
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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