A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155850



Internal ID22086355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12781785..12868035hg38UCSC Ensembl
Outerchr1:12779433..12923686hg38UCSC Ensembl
Innerchr1:12841928..12927856hg19UCSC Ensembl
Outerchr1:12839576..12983506hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38144254
hg19143931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015240, nssv4015251
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF10, PRAMEF11, PRAMEF2, PRAMEF4, PRAMEF7, PRAMEF8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155850
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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