A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509984



Internal ID20883297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91791936..91808597hg38UCSC Ensembl
chr15:92335166..92351827hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3816662
hg1916662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509984
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