A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156073



Internal ID22086578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86616161..86624971hg38UCSC Ensembl
Outerchr1:86607318..86634341hg38UCSC Ensembl
Innerchr1:87081844..87090654hg19UCSC Ensembl
Outerchr1:87073001..87100024hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3827024
hg1927024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017906
Samples
Known GenesCLCA3P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156073
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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