A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148218



Internal ID19200862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65242750..65254048hg38UCSC Ensembl
Outerchr9:42748499..42759800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3811299
hg1911302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001728
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148218
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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