A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792454



Internal ID18823801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19197559..19235496hg38UCSC Ensembl
Innerchr8:19055069..19093006hg19UCSC Ensembl
Innerchr8:19099349..19137286hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3837938
hg1937938
hg1837938
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891368
Supporting Variants
Samples
Known GenesLOC100128993
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792454
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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