A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855452



Internal ID22630387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113911237..113913236hg38UCSC Ensembl
chr13:114614210..114616209hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465337
Samples
Known GenesLINC00452
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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