A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792954



Internal ID19178700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68211285..68270705hg38UCSC Ensembl
Innerchr6:68921177..68980597hg19UCSC Ensembl
Innerchr6:68977898..69037318hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3859421
hg1959421
hg1859421
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890874
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792954
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer