A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150080



Internal ID19201474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70285348..70290749hg38UCSC Ensembl
Outerchr3:70334499..70339900hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998868
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150080
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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