A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146453



Internal ID19197915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68220683..68227884hg38UCSC Ensembl
Outerchr9:70835599..70842800hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg387202
hg197202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995607
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146453
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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