A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840356



Internal ID22615291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112323484..112355745hg38UCSC Ensembl
chr5:111659181..111691442hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3832262
hg1932262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493080
Samples
Known GenesEPB41L4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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