A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790341



Internal ID21235679
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 StatusM
Merged Variants
Supporting Variantsnssv13686746
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790341
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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