A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14250886



Internal ID1933388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100418907..100522989hg38UCSC Ensembl
chr11:100289638..100393720hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38104083
hg19104083
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627484
Supporting Variants
SamplesHG01801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14250886
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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