A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14245468



Internal ID5509337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97191702..97353386hg38UCSC Ensembl
chr11:97062702..97224386hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38161685
hg19161685
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627399
Supporting Variants
SamplesNA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14245468
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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