A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509503



Internal ID20882813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28452401..28753200hg38UCSC Ensembl
chr15:28697547..28998346hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38300800
hg19300800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177263
Samples
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer