A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066114



Internal ID1067930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87803120..87811260hg38UCSC Ensembl
Innerchr3:87803134..87811247hg38UCSC Ensembl
Outerchr3:87803107..87811274hg38UCSC Ensembl
chr3:87852270..87860410hg19UCSC Ensembl
Innerchr3:87852284..87860397hg19UCSC Ensembl
Outerchr3:87852257..87860424hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg388141
hg198141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596896
Supporting Variants
SamplesHG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066114
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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