A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150959



Internal ID19199439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50205060..50205176hg38UCSC Ensembl
Outerchr22:50643489..50643605hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001892
SamplesKWB1
Known GenesSELO
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150959
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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