A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154862



Internal ID22085367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:121669103..121694583hg38UCSC Ensembl
Outerchr12:121660606..121700223hg38UCSC Ensembl
Innerchr12:122107009..122132489hg19UCSC Ensembl
Outerchr12:122098512..122138129hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3839618
hg1939618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010308
Samples
Known GenesMORN3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154862
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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