A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7332n54



Internal ID22775227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230012456..230013398hg38UCSC Ensembl
chr2:230877172..230878114hg19UCSC Ensembl
chr2:230585416..230586358hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38943
hg19943
hg18943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584657, nsv584658
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7332n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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