A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986636



Internal ID20553676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118851403..118851662hg38UCSC Ensembl
chr11:118722112..118722371hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986636
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