A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785908



Internal ID19165249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153892457..153902233hg38UCSC Ensembl
Innerchr3:153610246..153620022hg19UCSC Ensembl
Innerchr3:155092936..155102712hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg389777
hg199777
hg189777
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893789
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785908
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