A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785385



Internal ID19176085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39472638hg38UCSC Ensembl
Innerchr8:39237668..39330157hg19UCSC Ensembl
Innerchr8:39356825..39449314hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3892490
hg1992490
hg1892490
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=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785385
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