A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv28e196



Internal ID22757698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:62506780..63239999hg38UCSC Ensembl
chr7:61887817..62700377hg19UCSC Ensembl
chr7:61525252..62337812hg18UCSC Ensembl
chr7:61331967..62144527hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38733220
hg19812561
hg18812561
hg17812561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422384, esv2422387
SamplesND04991, ND01692
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv28e196
Frequency
Sample Size181
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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