A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5914n100



Internal ID22792001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7425013..7452602hg38UCSC Ensembl
chr6:7425246..7452835hg19UCSC Ensembl
chr6:7370245..7397834hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3827590
hg1927590
hg1827590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024962, nsv1017007
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5914n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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