A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779417



Internal ID19163496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39416742..39499982hg38UCSC Ensembl
Innerchr8:39274261..39357501hg19UCSC Ensembl
Innerchr8:39393418..39476658hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3883241
hg1983241
hg1883241
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891382
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779417
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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