A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1045n106



Internal ID20160402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113802527..113803663hg38UCSC Ensembl
chr13:114505500..114506636hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141628, nsv1130143, nsv1128708
SamplesKWS1
Known GenesTMEM255B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1045n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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