A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5885n100



Internal ID22791972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:258253..328345hg38UCSC Ensembl
chr6:258253..328345hg19UCSC Ensembl
chr6:203253..273345hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3870093
hg1970093
hg1870093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030671, nsv1021606, nsv1019014, nsv1017206, nsv1033553, nsv1020407, nsv1016679
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)dgv5885n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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