A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv739n106



Internal ID20160096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132213718..132214043hg38UCSC Ensembl
chr11:132083612..132083937hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129907, nsv1111892, nsv1135604
SamplesKWS1, KWS2
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv739n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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