A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308902



Internal ID14809165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114228785..114228786hg38UCSC Ensembl
Innerchr7:114228725..114228846hg38UCSC Ensembl
Outerchr7:114228724..114228847hg38UCSC Ensembl
chr7:113868840..113868841hg19UCSC Ensembl
Innerchr7:113868780..113868901hg19UCSC Ensembl
Outerchr7:113868779..113868902hg19UCSC Ensembl
chr7:113656076..113656077hg18UCSC Ensembl
Innerchr7:113656137..113656016hg18UCSC Ensembl
Outerchr7:113656015..113656138hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3894
hg1994
hg1894
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838854
SamplesNA19238
Known GenesFOXP2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308902
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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