A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940644



Internal ID22716055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32867311..32881097hg38UCSC Ensembl
chr13:33441449..33455235hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3813787
hg1913787
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388382
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940644
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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