A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv668n106



Internal ID22794496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68415625..68415937hg38UCSC Ensembl
chr11:68183093..68183405hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113405, nsv1118419, nsv1111409
SamplesKWS2, KWS1
Known GenesLRP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv668n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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