A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985463



Internal ID20552503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102247242..102264751hg38UCSC Ensembl
chr11:102117973..102135482hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3817510
hg1917510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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