A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666978



Internal ID9933083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101378619..101380196hg38UCSC Ensembl
chr7:101021900..101023477hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381578
hg191578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5863311
SamplesNA19909
Known GenesCOL26A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666978
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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