A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502545



Internal ID20875791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68918701..68989100hg38UCSC Ensembl
chr15:69211040..69281439hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3870400
hg1970400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191244
Samples
Known GenesMIR548H4, NOX5, SPESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502545
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