A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683498



Internal ID21205357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1754500..1754500hg38UCSC Ensembl
chr11:1775730..1775730hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789958
Supporting Variants
Samples
Known GenesCTSD, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683498
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.166667


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