A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686746



Internal ID21208601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27517583..27517583hg38UCSC Ensembl
chr11:27539130..27539130hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790341
Supporting Variants
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686746
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.890625


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