A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940410



Internal ID22715819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108258230..108258479hg38UCSC Ensembl
chr13:108910578..108910827hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940410
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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