A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893743



Internal ID19184563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90230765..90259908hg38UCSC Ensembl
Outerchr3:90230765..90259908hg38UCSC Ensembl
Innerchr3:90279915..90309058hg19UCSC Ensembl
Outerchr3:90279915..90309058hg19UCSC Ensembl
Innerchr3:90362605..90391748hg18UCSC Ensembl
Outerchr3:90362605..90391748hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3829144
hg1929144
hg1829144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784918, essv25779962, essv25779629, essv25784681, essv25784632, essv25779897, essv25784796, essv25779845
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893743
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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