A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154790



Internal ID22085295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:667013..686965hg38UCSC Ensembl
Outerchr12:663075..689049hg38UCSC Ensembl
Innerchr12:776179..796131hg19UCSC Ensembl
Outerchr12:772241..798215hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3825975
hg1925975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv55n97
Supporting Variantsnssv4008332
Samples
Known GenesNINJ2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154790
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer