A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985608



Internal ID20552648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101879174..101881199hg38UCSC Ensembl
chr11:101749905..101751930hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985608
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