A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5910n100



Internal ID22791997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1268949..1328788hg38UCSC Ensembl
chr6:1269184..1329023hg19UCSC Ensembl
chr6:1214184..1274023hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3859840
hg1959840
hg1859840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026271, nsv1025058
Samples
Known GenesFOXQ1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5910n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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