A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848642



Internal ID22623577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77473168..77477814hg38UCSC Ensembl
chr13:78047303..78051949hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg384647
hg194647
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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