A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448117



Internal ID21105670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6421538..6464910hg38UCSC Ensembl
chr11:6442768..6486140hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3843373
hg1943373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191163
Samples
Known GenesHPX, TRIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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