A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066115



Internal ID1067931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87803460..87899387hg38UCSC Ensembl
chr3:87852610..87948537hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3895928
hg1995928
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596897
Supporting Variants
SamplesHG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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