A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786059



Internal ID19164319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115967306..115976722hg38UCSC Ensembl
Innerchr8:116979531..116988947hg19UCSC Ensembl
Innerchr8:117048709..117058125hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg389417
hg199417
hg189417
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891467
Supporting Variants
Samples
Known GenesLINC00536, MIR6507
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786059
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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