A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863101



Internal ID22638036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24030862..24031864hg38UCSC Ensembl
chr14:24500071..24501073hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465298, nssv17461674
Samples
Known GenesDHRS4L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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