A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7331n54



Internal ID22775226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230012354..230014629hg38UCSC Ensembl
chr2:230877070..230879345hg19UCSC Ensembl
chr2:230585314..230587589hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg382276
hg192276
hg182276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584662, nsv584656, nsv584661, nsv584660, nsv584665, nsv584655, nsv584664
Samples
Known GenesFBXO36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7331n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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