A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853819



Internal ID22628754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112681623..112684928hg38UCSC Ensembl
chr13:113335937..113339242hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383306
hg193306
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450716
Samples
Known GenesC13orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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