A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146046



Internal ID19196603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39787781..39819182hg38UCSC Ensembl
Outerchr9:41932799..41964200hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3831402
hg1931402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997410
SamplesKWB1
Known GenesKGFLP2, MGC21881
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146046
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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