A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190173



Internal ID20757213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13076578..13087339hg38UCSC Ensembl
chr11:13098125..13108886hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3810762
hg1910762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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