A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514686



Internal ID20888041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28174352..28679367hg38UCSC Ensembl
chr15:28419498..28924513hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38505016
hg19505016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194937
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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