A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690910



Internal ID21212764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134055478..134055478hg38UCSC Ensembl
chr11:133925373..133925373hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690910
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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