A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066129



Internal ID6939728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87824273..87825955hg38UCSC Ensembl
Innerchr3:87824286..87825943hg38UCSC Ensembl
Outerchr3:87824261..87825968hg38UCSC Ensembl
chr3:87873423..87875105hg19UCSC Ensembl
Innerchr3:87873436..87875093hg19UCSC Ensembl
Outerchr3:87873411..87875118hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596901
Supporting Variants
SamplesNA21126
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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