A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117206



Internal ID18933094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:307796..307860hg38UCSC Ensembl
Outerchr19:307796..307860hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979390
SamplesKWS2
Known GenesMIER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117206
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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