A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929282



Internal ID22704533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26065437..26085281hg38UCSC Ensembl
chr13:26639575..26659419hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3819845
hg1919845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929282
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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