A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473894



Internal ID21131447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122660937..122819103hg38UCSC Ensembl
chr11:122531645..122689811hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38158167
hg19158167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192646
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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