A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6086125



Internal ID9605034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93049591..93050382hg38UCSC Ensembl
chr9:95811873..95812664hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677695
Supporting Variants
SamplesNA19248
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6086125
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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