A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv607n106



Internal ID22794435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27635667..27636064hg38UCSC Ensembl
chr11:27657214..27657611hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120652, nsv1120043, nsv1130305
SamplesKWS2, KWS1
Known GenesBDNF-AS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv607n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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