A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7736386



Internal ID13093080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40915850..40915902hg38UCSC Ensembl
Outerchr7:40915650..40916102hg38UCSC Ensembl
Innerchr7:40955449..40955501hg19UCSC Ensembl
Outerchr7:40955249..40955701hg19UCSC Ensembl
Innerchr7:40921974..40922026hg18UCSC Ensembl
Outerchr7:40921774..40922226hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38453
hg19453
hg18453
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302832
Supporting Variants
SamplesNA10847
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7736386
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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