A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859908



Internal ID22634843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42682453..42686102hg38UCSC Ensembl
chr13:43256589..43260238hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg383650
hg193650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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