A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679632



Internal ID21201494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84099837..84099837hg38UCSC Ensembl
chr11:83810880..83810880hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791359
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.78125


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