A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1241n106



Internal ID22795069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73896202..73896278hg38UCSC Ensembl
chr15:74188543..74188619hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111119, nsv1125609
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1241n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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