A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv480n21



Internal ID22766672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14344889..14348564hg38UCSC Ensembl
chr9:14344888..14348563hg19UCSC Ensembl
chr9:14334888..14338563hg18UCSC Ensembl
chr9:14334888..14338563hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg383676
hg193676
hg183676
hg173676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523410, nsv527980
Samples
Known GenesNFIB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv480n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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