A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148724



Internal ID19195414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67363916..67371596hg38UCSC Ensembl
Outerchr9:40102399..40110100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg387681
hg197702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997513
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148724
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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