A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999927



Internal ID18848238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62288998..62291099hg38UCSC Ensembl
Outerchr9:46600299..46602400hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152743
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999927
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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