A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5899n100



Internal ID22791986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:330692..385772hg38UCSC Ensembl
chr6:330692..385772hg19UCSC Ensembl
chr6:275692..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3855081
hg1955081
hg1855081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030360, nsv1033859, nsv1017286, nsv1027634, nsv1023980, nsv1028112
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)dgv5899n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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