A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656997



Internal ID9923102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111957117..111957630hg38UCSC Ensembl
chr9:114719397..114719910hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6542129, essv6034901, essv5554463, essv5788297, essv5813076
SamplesHG01374, NA19381, NA19917, NA19722, NA19375
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656997
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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