A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463126



Internal ID21120679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59664401..59672300hg38UCSC Ensembl
chr11:59431874..59439773hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188757
Samples
Known GenesPATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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