A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891347



Internal ID19185743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14879753..15157646hg38UCSC Ensembl
Outerchr8:14762811..15249761hg38UCSC Ensembl
Innerchr8:14737262..15015155hg19UCSC Ensembl
Outerchr8:14620320..15107270hg19UCSC Ensembl
Innerchr8:14781633..15059526hg18UCSC Ensembl
Outerchr8:14664691..15151641hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38486951
hg19486951
hg18486951
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784719, essv25791077
Samples
Known GenesMIR383, SGCZ
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891347
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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