A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5903n100



Internal ID22791990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:346085..361143hg38UCSC Ensembl
chr6:346085..361143hg19UCSC Ensembl
chr6:291085..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3815059
hg1915059
hg1815059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021894, nsv1018725, nsv1022662, nsv1022993
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)dgv5903n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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