A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185224



Internal ID20752264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67083318..67098148hg38UCSC Ensembl
chr11:66850789..66865619hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3814831
hg1914831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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