A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932019



Internal ID22707311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82367904..82367982hg38UCSC Ensembl
chr13:82942039..82942117hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932019
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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