A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846099



Internal ID22621034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79515447..79516746hg38UCSC Ensembl
chr6:80225164..80226463hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508053, nssv17508054
Samples
Known GenesLCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846099
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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