A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788749



Internal ID19164954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26985012..27059034hg38UCSC Ensembl
Innerchr14:27454218..27528240hg19UCSC Ensembl
Innerchr14:26524058..26598080hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3874023
hg1974023
hg1874023
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892485
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788749
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