A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915623



Internal ID22690841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126375853..126397029hg38UCSC Ensembl
chr11:126245748..126266924hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3821177
hg1921177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351191
Samples
Known GenesST3GAL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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