A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854794



Internal ID22629729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51551632..51552681hg38UCSC Ensembl
chr13:52125768..52126817hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450424
Samples
Known GenesMIR4703
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854794
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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