A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5959n100



Internal ID22792046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48633854..48746539hg38UCSC Ensembl
chr6:48601590..48714176hg19UCSC Ensembl
chr6:48709549..48822135hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38112686
hg19112587
hg18112587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034217, nsv1015258
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)dgv5959n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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