A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5863311



Internal ID9808480
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 Flag1
Merged StatusS
Merged Variantsesv2666978
Supporting Variants
SamplesNA19909
Known GenesCOL26A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5863311
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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