A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948943



Internal ID21369012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128584984..128585076hg38UCSC Ensembl
chr11:128454879..128454971hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181336
SamplesHG002
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948943
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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