A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458343



Internal ID21115896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98794299..98795147hg38UCSC Ensembl
chr11:98665029..98665877hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458343
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