A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151598



Internal ID19200674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:16367189..16404172hg38UCSC Ensembl
Outerchr22:16847799..16884900hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3836984
hg1937102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003022
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151598
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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