A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460955



Internal ID21118508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122662901..122667200hg38UCSC Ensembl
chr11:122533609..122537908hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987643
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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