A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893864



Internal ID19184684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5286432..5362401hg38UCSC Ensembl
Outerchr4:5286432..5362401hg38UCSC Ensembl
Innerchr4:5288159..5364128hg19UCSC Ensembl
Outerchr4:5288159..5364128hg19UCSC Ensembl
Innerchr4:5339060..5415029hg18UCSC Ensembl
Outerchr4:5339060..5415029hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3875970
hg1975970
hg1875970
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790218
Samples
Known GenesSTK32B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893864
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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