A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683289



Internal ID21205147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055105..36055105hg38UCSC Ensembl
chr11:36076655..36076655hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790377
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683289
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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