A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3834n106



Internal ID22797662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61995541..62000341hg38UCSC Ensembl
chr8:62908100..62912900hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1128976, nsv1125014
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3834n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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