A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893680



Internal ID19184500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30231029..30299934hg38UCSC Ensembl
Outerchr3:30226266..30299934hg38UCSC Ensembl
Innerchr3:30272520..30341425hg19UCSC Ensembl
Outerchr3:30267757..30341425hg19UCSC Ensembl
Innerchr3:30247524..30316429hg18UCSC Ensembl
Outerchr3:30242761..30316429hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3873669
hg1973669
hg1873669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799949, essv25800341, essv25784154, essv25799734, essv25786997, essv25796656, essv25782826, essv25781846, essv25801209, essv25801586, essv25795991, essv25785157, essv25781362, essv25787705, essv25798805, essv25787522, essv25779699, essv25796433, essv25782145
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893680
Frequency
Sample Size3017
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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