A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787918



Internal ID19160416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14962453..15018884hg38UCSC Ensembl
Innerchr10:15004452..15060883hg19UCSC Ensembl
Innerchr10:15044458..15100889hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3856432
hg1956432
hg1856432
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891763
Supporting Variants
Samples
Known GenesMEIG1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787918
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