A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472215



Internal ID21129768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128545236..128545895hg38UCSC Ensembl
chr11:128415131..128415790hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987489
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472215
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