A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893628



Internal ID19184448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093768..4171349hg38UCSC Ensembl
Outerchr3:4080585..4204149hg38UCSC Ensembl
Innerchr3:4135452..4213033hg19UCSC Ensembl
Outerchr3:4122269..4245833hg19UCSC Ensembl
Innerchr3:4110452..4188033hg18UCSC Ensembl
Outerchr3:4097269..4220833hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38123565
hg19123565
hg18123565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783437, essv25784140, essv25780795, essv25796234, essv25800879, essv25783092, essv25799817, essv25796853, essv25780013, essv25796917, essv25800983, essv25796401, essv25798416, essv25783852, essv25780100, essv25778511, essv25781343, essv25801632, essv25780590, essv25780048, essv25784245, essv25796369, essv25784618, essv25801127, essv25801106, essv25796094, essv25781863, essv25785281, essv25786258, essv25779089
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893628
Frequency
Sample Size3017
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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