A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893631



Internal ID18837765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4151816..4245016hg38UCSC Ensembl
Outerchr3:4119651..4283616hg38UCSC Ensembl
Innerchr3:4193500..4286700hg19UCSC Ensembl
Outerchr3:4161335..4325300hg19UCSC Ensembl
Innerchr3:4168500..4261700hg18UCSC Ensembl
Outerchr3:4136335..4300300hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38163966
hg19163966
hg18163966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785019, essv25787696, essv25785960
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893631
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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