A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14095036



Internal ID4194392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37932633..38000019hg38UCSC Ensembl
chr11:37954183..38021569hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3867387
hg1967387
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625997
Supporting Variants
SamplesHG03782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14095036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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