A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179106



Internal ID20746146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112201101..112236800hg38UCSC Ensembl
chr11:112071824..112107523hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3835700
hg1935700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474741
Supporting Variants
Samples
Known GenesBCO2, PTS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00064


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