A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625772



Internal ID7012606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27539296..27551984hg38UCSC Ensembl
Innerchr11:27539446..27551834hg38UCSC Ensembl
Outerchr11:27539146..27552134hg38UCSC Ensembl
chr11:27560843..27573531hg19UCSC Ensembl
Innerchr11:27560993..27573381hg19UCSC Ensembl
Outerchr11:27560693..27573681hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3812689
hg1912689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14071758
SamplesHG00614
Known GenesBDNF-AS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625772
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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