A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5988n100



Internal ID22792075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61139432..61260227hg38UCSC Ensembl
chr6:61977487..62098282hg19UCSC Ensembl
chr6:62035446..62156241hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38120796
hg19120796
hg18120796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031766, nsv1017584
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)dgv5988n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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