A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471876



Internal ID22529768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44507035..44538368hg38UCSC Ensembl
chr15:44799233..44830566hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3831334
hg1931334
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852913
Supporting Variants
Samples
Known GenesCTDSPL2, EIF3J, EIF3J-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471876
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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