A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508390



Internal ID20881690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35334101..35338600hg38UCSC Ensembl
chr15:35626302..35630801hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer