A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989130



Internal ID20556170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26584149..26586412hg38UCSC Ensembl
chr11:26605696..26607959hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382264
hg192264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450080
Supporting Variants
Samples
Known GenesANO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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