A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028877



Internal ID21938220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40050450..40050555hg38UCSC Ensembl
chr15:40342651..40342756hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598591
Samples
Known GenesSRP14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028877
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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