A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987115



Internal ID20554157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116805575..116820181hg38UCSC Ensembl
chr11:116676291..116690897hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3814607
hg1914607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987115
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