A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457194



Internal ID21114747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117325028..117356139hg38UCSC Ensembl
chr11:117195744..117226855hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3831112
hg1931112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196786
Samples
Known GenesCEP164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457194
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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