A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891477



Internal ID19185873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125470898..125492484hg38UCSC Ensembl
Outerchr8:125470898..125492484hg38UCSC Ensembl
Innerchr8:126483140..126504726hg19UCSC Ensembl
Outerchr8:126483140..126504726hg19UCSC Ensembl
Innerchr8:126552322..126573908hg18UCSC Ensembl
Outerchr8:126552322..126573908hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3821587
hg1921587
hg1821587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784665
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891477
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