A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008331



Internal ID22069962
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154789
Supporting Variants
Samples
Known GenesNINJ2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008331
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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