A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891368



Internal ID18839078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19197559..19227662hg38UCSC Ensembl
Outerchr8:19192301..19235496hg38UCSC Ensembl
Innerchr8:19055069..19085172hg19UCSC Ensembl
Outerchr8:19049811..19093006hg19UCSC Ensembl
Innerchr8:19099349..19129452hg18UCSC Ensembl
Outerchr8:19094091..19137286hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3843196
hg1943196
hg1843196
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781597, essv25792454
Samples
Known GenesLOC100128993
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891368
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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