A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692918



Internal ID21214770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69111015..69111015hg38UCSC Ensembl
chr11:68878483..68878483hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692918
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.953125


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