A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv487n21



Internal ID20132208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74485743..74549090hg38UCSC Ensembl
chr9:77100659..77164006hg19UCSC Ensembl
chr9:76290479..76353826hg18UCSC Ensembl
chr9:74330213..74393560hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3863348
hg1963348
hg1863348
hg1763348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527927, nsv528271
Samples
Known GenesMIR6130, RORB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv487n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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