A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452283



Internal ID22510156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126364142..126372053hg38UCSC Ensembl
chr11:126234037..126241948hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg387912
hg197912
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852467
Supporting Variants
Samples
Known GenesST3GAL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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