A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154730



Internal ID22085235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21994018..22010750hg38UCSC Ensembl
Outerchr1:21992508..22011632hg38UCSC Ensembl
Innerchr1:22320511..22337243hg19UCSC Ensembl
Outerchr1:22319001..22338125hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3819125
hg1919125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007073
Samples
Known GenesCELA3A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154730
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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