A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861841



Internal ID22636776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27632638..27633710hg38UCSC Ensembl
chr11:27654185..27655257hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381073
hg191073
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466374, nssv17462870
Samples
Known GenesBDNF-AS, LINC00678
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861841
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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