A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151813



Internal ID19202222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9913371..10009872hg38UCSC Ensembl
Outerchr21:10391399..10487900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3896502
hg1996502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998995
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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