A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997513



Internal ID19191119
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 StatusS
Merged Variantsnsv1148724
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997513
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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