A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033226



Internal ID21942569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88117590..88471253hg38UCSC Ensembl
chr15:88660821..89014484hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38353664
hg19353664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600021
Samples
Known GenesMRPL46, MRPS11, NTRK3, NTRK3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033226
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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