A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151438



Internal ID19202332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:8819266..8845567hg38UCSC Ensembl
Outerchr21:9708099..9734400hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3826302
hg1926302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004001
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151438
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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