A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921103



Internal ID22696326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118685271..118685349hg38UCSC Ensembl
chr10:120444783..120444861hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356316
Samples
Known GenesCACUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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