A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856597



Internal ID22631532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19177557..19189210hg38UCSC Ensembl
chr13:19751697..19763350hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3811654
hg1911654
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464608
Samples
Known GenesTUBA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856597
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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