A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547509



Internal ID18748585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27635771..27636042hg38UCSC Ensembl
Outerchr11:27635701..27636059hg38UCSC Ensembl
Innerchr11:27657318..27657589hg19UCSC Ensembl
Outerchr11:27657248..27657606hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746256
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547509
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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