A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153412



Internal ID19196916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98001069..98002870hg38UCSC Ensembl
Outerchr15:98544299..98546100hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001331
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153412
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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