A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5881n100



Internal ID22791968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:253861..303121hg38UCSC Ensembl
chr6:253861..303121hg19UCSC Ensembl
chr6:198861..248121hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849261
hg1949261
hg1849261
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027013, nsv1024786, nsv1016091, nsv1015833, nsv1026036, nsv1033176, nsv1025559, nsv1018010, nsv1033541, nsv1018768, nsv1030065
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)dgv5881n100
Frequency
Sample Size11257
Observed Gain79
Observed Loss413
Observed Complex0
Frequencyn/a


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