A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7742712



Internal ID14665225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128826789..128826790hg38UCSC Ensembl
Innerchr10:128826762..128826817hg38UCSC Ensembl
Outerchr10:128826761..128826818hg38UCSC Ensembl
chr10:130625053..130625054hg19UCSC Ensembl
Innerchr10:130625026..130625081hg19UCSC Ensembl
Outerchr10:130625025..130625082hg19UCSC Ensembl
chr10:130515043..130515044hg18UCSC Ensembl
Innerchr10:130515071..130515016hg18UCSC Ensembl
Outerchr10:130515015..130515072hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386015
hg196015
hg186015
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306270
Supporting Variants
SamplesNA18964
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7742712
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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