A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066123



Internal ID1985806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87820260..87823510hg38UCSC Ensembl
Innerchr3:87820260..87823510hg38UCSC Ensembl
Outerchr3:87820177..87823539hg38UCSC Ensembl
chr3:87869410..87872660hg19UCSC Ensembl
Innerchr3:87869410..87872660hg19UCSC Ensembl
Outerchr3:87869327..87872689hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596900
Supporting Variants
SamplesHG01845
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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