A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942426



Internal ID22717863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42708329..42715686hg38UCSC Ensembl
chr13:43282465..43289822hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg387358
hg197358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942426
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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