A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6310556



Internal ID9287959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111970516..111970759hg38UCSC Ensembl
chr9:114732796..114733039hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660384
Supporting Variants
SamplesNA19093
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6310556
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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