A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3769n106



Internal ID22797597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9594639..9596990hg38UCSC Ensembl
chr8:9452149..9454500hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1123622, nsv1129404
SamplesKWS1
Known GenesTNKS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3769n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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