A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5983n100



Internal ID22792070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61274104..61350771hg38UCSC Ensembl
chr6:61886428..61963609hg19UCSC Ensembl
chr6:61944387..62021568hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3876668
hg1977182
hg1877182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022375, nsv1024924
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)dgv5983n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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