A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853715



Internal ID22628650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67368539..67381724hg38UCSC Ensembl
chr13:67942671..67955856hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3813186
hg1913186
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853715
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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