A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094947



Internal ID22004180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27517582..27517582hg38UCSC Ensembl
chr11:27539129..27539129hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588437
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094947
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer