A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859221



Internal ID22634156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60688891..60692315hg38UCSC Ensembl
chr13:61263025..61266449hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463361
Samples
Known GenesLINC00378
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859221
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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