A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5909911



Internal ID8855879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81806344..81808336hg38UCSC Ensembl
chr9:84421259..84423251hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670502
Supporting Variants
SamplesHG00311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5909911
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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