A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467334



Internal ID21124887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126280496..126285969hg38UCSC Ensembl
chr11:126150391..126155864hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385474
hg195474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195795
Samples
Known GenesTIRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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