A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6222071



Internal ID9759406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17893417..17894907hg38UCSC Ensembl
chr8:17750926..17752416hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381491
hg191491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664484
Supporting Variants
SamplesNA19713
Known GenesFGL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6222071
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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