A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596888



Internal ID6984202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87398492..87407399hg38UCSC Ensembl
Innerchr3:87398492..87407399hg38UCSC Ensembl
Outerchr3:87398334..87407611hg38UCSC Ensembl
chr3:87447642..87456549hg19UCSC Ensembl
Innerchr3:87447642..87456549hg19UCSC Ensembl
Outerchr3:87447484..87456761hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg388908
hg198908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063997, essv11064002, essv11063999, essv11063998, essv11064003, essv11064004, essv11063995, essv11063996, essv11064000, essv11064001
SamplesHG03096, HG01064, HG02756, HG03479, NA19451, NA19449, NA19019, NA19428, NA19472, NA19316
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596888
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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