A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2237n106



Internal ID22796065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31216079..31246697hg38UCSC Ensembl
chr20:29803900..29834500hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3830619
hg1930601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110370, nsv1115601
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2237n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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