A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10264n54



Internal ID22778159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:296257..381918hg38UCSC Ensembl
chr6:296257..381918hg19UCSC Ensembl
chr6:241257..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3885662
hg1985662
hg1885662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600766, nsv600768, nsv600769, nsv600771, nsv600765, nsv600767, nsv600772
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10264n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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