A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843703



Internal ID22618638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11014253..11015649hg38UCSC Ensembl
chr6:11014486..11015882hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501061
Samples
Known GenesELOVL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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