A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182323



Internal ID20749363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60209359..60251775hg38UCSC Ensembl
chr11:59976832..60019248hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3842417
hg1942417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472356
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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