A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780833



Internal ID19175959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6440687..6524190hg38UCSC Ensembl
Innerchr3:6482374..6565877hg19UCSC Ensembl
Innerchr3:6457374..6540877hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3883504
hg1983504
hg1883504
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893651
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780833
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