A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893859



Internal ID19184679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:421522..481679hg38UCSC Ensembl
Outerchr4:416226..503349hg38UCSC Ensembl
Innerchr4:415311..475468hg19UCSC Ensembl
Outerchr4:410015..497138hg19UCSC Ensembl
Innerchr4:405311..465468hg18UCSC Ensembl
Outerchr4:400015..487138hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3887124
hg1987124
hg1887124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789432, essv25792743, essv25791412
Samples
Known GenesABCA11P, PIGG, ZNF721
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893859
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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