A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780377



Internal ID18833189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14808160..14845522hg38UCSC Ensembl
Innerchr3:14849667..14887029hg19UCSC Ensembl
Innerchr3:14824671..14862033hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3837363
hg1937363
hg1837363
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893664
Supporting Variants
Samples
Known GenesFGD5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780377
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