A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780548



Internal ID19161819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092262..16163959hg38UCSC Ensembl
Innerchr8:15949771..16021468hg19UCSC Ensembl
Innerchr8:15994142..16065839hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3871698
hg1971698
hg1871698
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891356
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780548
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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