A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154085



Internal ID19195377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:198226628..198234529hg38UCSC Ensembl
Outerchr3:197953499..197961400hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387902
hg197902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003362
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154085
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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