A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153583



Internal ID19201583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62250098..62253199hg38UCSC Ensembl
Outerchr9:46561399..46564500hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002242
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153583
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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