A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435653



Internal ID21093206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5502286..5526914hg38UCSC Ensembl
chr11:5523516..5548144hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824629
hg1924629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194538
Samples
Known GenesOR51B5, UBQLN3, UBQLNL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435653
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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