A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6013n100



Internal ID22792100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:67835409..67932853hg38UCSC Ensembl
chr6:68545302..68642745hg19UCSC Ensembl
chr6:68602023..68699466hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3897445
hg1997444
hg1897444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030673, nsv1027600
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)dgv6013n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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