A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456023



Internal ID21113576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65065542..65073199hg38UCSC Ensembl
chr11:64833014..64840671hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387658
hg197658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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