A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154854



Internal ID22085359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:107191436..107260140hg38UCSC Ensembl
Outerchr12:107185827..107261371hg38UCSC Ensembl
Innerchr12:107585214..107653918hg19UCSC Ensembl
Outerchr12:107579605..107655149hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3875545
hg1975545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010296
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154854
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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