A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678116



Internal ID9944221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110216066..110235372hg38UCSC Ensembl
chr7:109856123..109875429hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3819307
hg1919307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5748115
SamplesHG00596
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678116
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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