A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6141n100



Internal ID22792228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117406387..117420332hg38UCSC Ensembl
chr6:117727550..117741495hg19UCSC Ensembl
chr6:117834243..117848188hg18UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3813946
hg1913946
hg1813946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025551, nsv1032651
Samples
Known GenesROS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6141n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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