A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5993417



Internal ID8898376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90410380..90412753hg38UCSC Ensembl
chr9:93172662..93175035hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382374
hg192374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677173
Supporting Variants
SamplesHG00346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5993417
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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