A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472878



Internal ID21130431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114611485..114677839hg38UCSC Ensembl
chr11:114482207..114548561hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3866355
hg1966355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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