A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436192



Internal ID21093745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17017284..17024588hg38UCSC Ensembl
chr11:17038831..17046135hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387305
hg197305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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