A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852281



Internal ID22627216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99188201..99197759hg38UCSC Ensembl
chr13:99840455..99850013hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg389559
hg199559
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467022
Samples
Known GenesUBAC2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852281
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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