A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241872



Internal ID4060240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94885697..94891286hg38UCSC Ensembl
chr11:94618862..94624451hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385590
hg195590
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627332
Supporting Variants
SamplesHG03696
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241872
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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