A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139614



Internal ID18931344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20815371..20835771hg38UCSC Ensembl
Outerchr15:21020700..21041100hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820401
hg1920401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1158n106
Supporting Variantsnssv3977200
SamplesKWS2
Known GenesPOTEB, POTEB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139614
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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