A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470193



Internal ID21127746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94613869..94615784hg38UCSC Ensembl
chr11:94347035..94348950hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381916
hg191916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191521
Samples
Known GenesPIWIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470193
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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