A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854064



Internal ID22628999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99371930..99375174hg38UCSC Ensembl
chr13:100024184..100027428hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383245
hg193245
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467086
Samples
Known GenesMIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854064
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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