A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2308n106



Internal ID22796136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10010272..10169772hg38UCSC Ensembl
chr21:10488300..10647800hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38159501
hg19159501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118674, nsv1141399
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2308n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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