A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505148



Internal ID20878414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67917280..67929674hg38UCSC Ensembl
chr15:68209618..68222012hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3812395
hg1912395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505148
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