A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156074



Internal ID22086579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197327674..197627117hg38UCSC Ensembl
Outerchr3:197322591..197659410hg38UCSC Ensembl
Innerchr3:197054545..197353988hg19UCSC Ensembl
Outerchr3:197049462..197386281hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38336820
hg19336820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n97
Supporting Variantsnssv4017357
Samples
Known GenesBDH1, LOC220729
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156074
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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