A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153899



Internal ID19196406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:131698259..131714060hg38UCSC Ensembl
Outerchr6:132019399..132035200hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3815802
hg1915802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003172
SamplesKWB1
Known GenesCTAGE9, ENPP3, OR2A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153899
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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