A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147549



Internal ID19202930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40782971..40875672hg38UCSC Ensembl
Outerchr9:66735999..66828700hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3892702
hg1992702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000326
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147549
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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