A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789889



Internal ID21235227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128585004..128585083hg38UCSC Ensembl
chr11:128454899..128454978hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv52n137
Supporting Variantsnssv13688981
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789889
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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