A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv740n106



Internal ID19018849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132688692..132689015hg38UCSC Ensembl
chr11:132558587..132558910hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120664, nsv1135446
SamplesKWS2
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv740n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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