A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153159



Internal ID18856005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:17801148..17801465hg38UCSC Ensembl
Outerchr22:18283914..18284231hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001074
SamplesKWB1
Known GenesMICAL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153159
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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