A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890887



Internal ID19185283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78025956..78063157hg38UCSC Ensembl
Outerchr6:78025956..78063157hg38UCSC Ensembl
Innerchr6:78735673..78772874hg19UCSC Ensembl
Outerchr6:78735673..78772874hg19UCSC Ensembl
Innerchr6:78792392..78829593hg18UCSC Ensembl
Outerchr6:78792392..78829593hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3837202
hg1937202
hg1837202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783332
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890887
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