A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941595



Internal ID22717022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105316240..105331117hg38UCSC Ensembl
chr13:105968591..105983468hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3814878
hg1914878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941595
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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