A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781382



Internal ID19173510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9101548..9150641hg38UCSC Ensembl
Innerchr10:9143511..9192604hg19UCSC Ensembl
Innerchr10:9183517..9232610hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3849094
hg1949094
hg1849094
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891753
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781382
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