A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv426n106



Internal ID22794254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42097572..42105055hg38UCSC Ensembl
chr10:42596699..42600503hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387484
hg193805
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116644, nsv1120218
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv426n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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