A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890874



Internal ID19185176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68211285..68270705hg38UCSC Ensembl
Outerchr6:68211285..68270705hg38UCSC Ensembl
Innerchr6:68921177..68980597hg19UCSC Ensembl
Outerchr6:68921177..68980597hg19UCSC Ensembl
Innerchr6:68977898..69037318hg18UCSC Ensembl
Outerchr6:68977898..69037318hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3859421
hg1959421
hg1859421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792954
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890874
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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