A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv676n106



Internal ID20160033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74821359..74821681hg38UCSC Ensembl
chr11:74532404..74532726hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134952, nsv1135441, nsv1120660
SamplesKWS1, KWS2
Known GenesRNF169
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv676n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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