A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890797



Internal ID19185099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21805483..21814560hg38UCSC Ensembl
Outerchr6:21805483..21814560hg38UCSC Ensembl
Innerchr6:21805714..21814791hg19UCSC Ensembl
Outerchr6:21805714..21814791hg19UCSC Ensembl
Innerchr6:21913693..21922770hg18UCSC Ensembl
Outerchr6:21913693..21922770hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389078
hg199078
hg189078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783117
Samples
Known GenesCASC15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890797
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