A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890889



Internal ID19185285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78354667..78453746hg38UCSC Ensembl
Outerchr6:78354667..78453746hg38UCSC Ensembl
Innerchr6:79064384..79163463hg19UCSC Ensembl
Outerchr6:79064384..79163463hg19UCSC Ensembl
Innerchr6:79121103..79220182hg18UCSC Ensembl
Outerchr6:79121103..79220182hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3899080
hg1999080
hg1899080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781221
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890889
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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