A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852913



Internal ID22627848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44507035..44538368hg38UCSC Ensembl
chr15:44799233..44830566hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3831334
hg1931334
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471876
Samples
Known GenesCTDSPL2, EIF3J, EIF3J-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852913
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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