A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684934



Internal ID21206790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125426490..125426614hg38UCSC Ensembl
chr11:125296386..125296510hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789754
Supporting Variants
Samples
Known GenesPKNOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684934
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.421875


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