A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154789



Internal ID22085294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:663075..689049hg38UCSC Ensembl
Outerchr12:662511..691425hg38UCSC Ensembl
Innerchr12:772241..798215hg19UCSC Ensembl
Outerchr12:771677..800591hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3828915
hg1928915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv55n97
Supporting Variantsnssv4008331
Samples
Known GenesNINJ2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154789
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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