A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519770



Internal ID20893131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47985386..47988474hg38UCSC Ensembl
chr17:46062752..46065840hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383089
hg193089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519770
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