A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8968662



Internal ID14127022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62793830..62793841hg38UCSC Ensembl
Innerchr15:62793823..62793848hg38UCSC Ensembl
Outerchr15:62793812..62793859hg38UCSC Ensembl
chr15:63086029..63086040hg19UCSC Ensembl
Innerchr15:63086022..63086047hg19UCSC Ensembl
Outerchr15:63086011..63086058hg19UCSC Ensembl
chr15:60873082..60873093hg18UCSC Ensembl
Innerchr15:60873100..60873075hg18UCSC Ensembl
Outerchr15:60873064..60873111hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3403298
Supporting Variants
SamplesNA18942
Known GenesTLN2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8968662
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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