A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5984n100



Internal ID22792071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61114361..61350771hg38UCSC Ensembl
chr6:61886428..62123350hg19UCSC Ensembl
chr6:61944387..62181309hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38236411
hg19236923
hg18236923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029624, nsv1019336, nsv1020044
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)dgv5984n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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