A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156146



Internal ID22086651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39584941..39587542hg38UCSC Ensembl
Outerchr4:39576456..39596035hg38UCSC Ensembl
Innerchr4:39586561..39589162hg19UCSC Ensembl
Outerchr4:39578076..39597655hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3819580
hg1919580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014237
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156146
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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