A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5667942



Internal ID8645345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91073348..91073431hg38UCSC Ensembl
chr9:93835630..93835713hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666630
Supporting Variants
SamplesNA19379
Known GenesLOC100129316
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5667942
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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