A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5890n100



Internal ID22791977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:285695..381137hg38UCSC Ensembl
chr6:285695..381137hg19UCSC Ensembl
chr6:230695..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3895443
hg1995443
hg1895443
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015536, nsv1022729, nsv1025947, nsv1033145, nsv1023381, nsv1024254, nsv1021626
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)dgv5890n100
Frequency
Sample Size11257
Observed Gain78
Observed Loss34
Observed Complex0
Frequencyn/a


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