A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455852



Internal ID22513729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122732806..122742078hg38UCSC Ensembl
chr11:122603514..122612786hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg389273
hg199273
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858997
Supporting Variants
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455852
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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