A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151039



Internal ID19202185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:18779186..18839587hg38UCSC Ensembl
Outerchr22:18766699..18827100hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3860402
hg1960402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001973
SamplesKWB1
Known GenesGGT3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151039
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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