A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891279



Internal ID19185675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3311753..4376584hg38UCSC Ensembl
Outerchr8:3311753..4376584hg38UCSC Ensembl
Innerchr8:3169275..4234106hg19UCSC Ensembl
Outerchr8:3169275..4234106hg19UCSC Ensembl
Innerchr8:3156682..4221514hg18UCSC Ensembl
Outerchr8:3156682..4221514hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg381064832
hg191064832
hg181064833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792019
Samples
Known GenesCSMD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891279
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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