A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505212



Internal ID20878478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35004674..35008010hg38UCSC Ensembl
chr15:35296875..35300211hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505212
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