A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010299



Internal ID22071930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:114194398..114200104hg38UCSC Ensembl
Outerchr12:114193597..114201059hg38UCSC Ensembl
Innerchr12:114632203..114637909hg19UCSC Ensembl
Outerchr12:114631402..114638864hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg387463
hg197463
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154857
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010299
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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