A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865148



Internal ID22640083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27629546..27634540hg38UCSC Ensembl
chr11:27651093..27656087hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg384995
hg194995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460258
Samples
Known GenesBDNF-AS, LINC00678
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865148
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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