A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893630



Internal ID18837764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4204149..4232962hg38UCSC Ensembl
Outerchr3:4204149..4234996hg38UCSC Ensembl
Innerchr3:4245833..4274646hg19UCSC Ensembl
Outerchr3:4245833..4276680hg19UCSC Ensembl
Innerchr3:4220833..4249646hg18UCSC Ensembl
Outerchr3:4220833..4251680hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3830848
hg1930848
hg1830848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778809, essv25781921, essv25783868, essv25779567
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893630
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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