A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496008



Internal ID20869206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47405997..47406408hg38UCSC Ensembl
chr15:47698194..47698605hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182007
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496008
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