A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859555



Internal ID22634490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35571983..35579273hg38UCSC Ensembl
chr13:36146120..36153410hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387291
hg197291
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461061
Samples
Known GenesMIR548F5, NBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859555
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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