A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843266



Internal ID22618201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88338381..88345280hg38UCSC Ensembl
chr5:87634198..87641097hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499505
Samples
Known GenesTMEM161B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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