A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785689



Internal ID19163817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39393511..39483411hg38UCSC Ensembl
Innerchr8:39251030..39340930hg19UCSC Ensembl
Innerchr8:39370187..39460087hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3889901
hg1989901
hg1889901
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891383
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785689
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