A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3869n106



Internal ID22797697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623072..101624772hg38UCSC Ensembl
chr8:102635300..102637000hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1132675, nsv1141593
SamplesKWS2, KWS1
Known GenesGRHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3869n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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