A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681118



Internal ID21202977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128585004..128585095hg38UCSC Ensembl
chr11:128454899..128454990hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789540
Supporting Variants
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681118
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.828125


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