A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3790n106



Internal ID19021899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18618180..18618643hg38UCSC Ensembl
chr8:18475690..18476153hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1131836, nsv1139125
SamplesKWS1
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3790n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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