A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596955



Internal ID6637225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89374998..89380341hg38UCSC Ensembl
Innerchr3:89375019..89380321hg38UCSC Ensembl
Outerchr3:89374978..89380362hg38UCSC Ensembl
chr3:89424148..89429491hg19UCSC Ensembl
Innerchr3:89424169..89429471hg19UCSC Ensembl
Outerchr3:89424128..89429512hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg385344
hg195344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068876
SamplesHG02455
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596955
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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