A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891864



Internal ID19186260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78556270..78596686hg38UCSC Ensembl
Outerchr10:78556270..78596686hg38UCSC Ensembl
Innerchr10:80316027..80356443hg19UCSC Ensembl
Outerchr10:80316027..80356443hg19UCSC Ensembl
Innerchr10:79986033..80026449hg18UCSC Ensembl
Outerchr10:79986033..80026449hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3840417
hg1940417
hg1840417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792897
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891864
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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