A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5879n100



Internal ID22791966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:252772..294825hg38UCSC Ensembl
chr6:252772..294825hg19UCSC Ensembl
chr6:197772..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842054
hg1942054
hg1842054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015154, nsv1023720, nsv1023416, nsv1023067, nsv1024077, nsv1033480, nsv1026405, nsv1031519
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5879n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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