A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843109



Internal ID22618044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60374767..60376450hg38UCSC Ensembl
chr5:59670594..59672277hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497445
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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