A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614456



Internal ID6654662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107206087..107217855hg38UCSC Ensembl
Innerchr7:107206118..107217825hg38UCSC Ensembl
Outerchr7:107206057..107217886hg38UCSC Ensembl
chr7:106846532..106858300hg19UCSC Ensembl
Innerchr7:106846563..106858270hg19UCSC Ensembl
Outerchr7:106846502..106858331hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3811769
hg1911769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917697
SamplesHG00683
Known GenesCOG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614456
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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