A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11160807



Internal ID6316849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138887938..138902075hg38UCSC Ensembl
chr3:138606780..138620917hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3814138
hg1914138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597927
Supporting Variants
SamplesNA19916
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11160807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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