A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2231n106



Internal ID22796059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25752564..25777864hg38UCSC Ensembl
chr20:25733200..25758500hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3825301
hg1925301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141380, nsv1132528
SamplesKWS2, KWS1
Known GenesFAM182B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2231n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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