A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510482



Internal ID20883801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17014001..17017400hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2362n223
Supporting Variantsnssv18023249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510482
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