A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470484



Internal ID21128037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68766766..68768282hg38UCSC Ensembl
chr11:68534234..68535750hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992675
Samples
Known GenesCPT1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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