A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778258



Internal ID18827048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20127871..20164378hg38UCSC Ensembl
Innerchr8:19985382..20021889hg19UCSC Ensembl
Innerchr8:20029662..20066169hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836508
hg1936508
hg1836508
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891373
Supporting Variants
Samples
Known GenesSLC18A1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778258
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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