A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875322



Internal ID22650279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47022976..47043592hg38UCSC Ensembl
chr18:44549424..44569963hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3820617
hg1920540
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478507
Samples
Known GenesKATNAL2, TCEB3B, TCEB3C, TCEB3CL, TCEB3CL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875322
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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