A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463854



Internal ID21121407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59668401..59670100hg38UCSC Ensembl
chr11:59435874..59437573hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182504
Samples
Known GenesPATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463854
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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