A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178058



Internal ID20745098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28642501..29119300hg38UCSC Ensembl
chr15:28887647..29411503hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38476800
hg19523857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511536
Supporting Variants
Samples
Known GenesAPBA2, GOLGA6L7P, GOLGA8M, HERC2P9, LOC100289656, LOC646278, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178058
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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