A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841387



Internal ID22616322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123783422..123784521hg38UCSC Ensembl
chr5:123119116..123120215hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494088, nssv17494089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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