A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155807



Internal ID22086312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:48043087..48118238hg38UCSC Ensembl
Outerchr22:48042468..48120774hg38UCSC Ensembl
Innerchr22:48438904..48514055hg19UCSC Ensembl
Outerchr22:48438285..48516591hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3878307
hg1978307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012946
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155807
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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