A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893692



Internal ID18837826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46766277..46802757hg38UCSC Ensembl
Outerchr3:46754860..46809120hg38UCSC Ensembl
Innerchr3:46807767..46844247hg19UCSC Ensembl
Outerchr3:46796350..46850610hg19UCSC Ensembl
Innerchr3:46782771..46819251hg18UCSC Ensembl
Outerchr3:46771354..46825614hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854261
hg1954261
hg1854261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783084, essv25779796, essv25779971, essv25786770, essv25798702, essv25779697, essv25781617, essv25781561, essv25784522, essv25782477, essv25778562, essv25782574, essv25780822, essv25798374, essv25779608, essv25799887, essv25783658, essv25783897, essv25781644
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893692
Frequency
Sample Size3017
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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