A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3789n106



Internal ID19021898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18597101..18598438hg38UCSC Ensembl
chr8:18454611..18455948hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135700, nsv1111733, nsv1131834
SamplesKWS1, KWS2
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3789n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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