A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850364



Internal ID22625299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45088251..45091862hg38UCSC Ensembl
chr13:45662386..45665997hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg383612
hg193612
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850364
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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