A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3304136



Internal ID14804398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32821096..32821097hg38UCSC Ensembl
Innerchr15:32821074..32821119hg38UCSC Ensembl
Outerchr15:32821073..32821120hg38UCSC Ensembl
chr15:33113297..33113298hg19UCSC Ensembl
Innerchr15:33113275..33113320hg19UCSC Ensembl
Outerchr15:33113274..33113321hg19UCSC Ensembl
chr15:30900589..30900590hg18UCSC Ensembl
Innerchr15:30900612..30900567hg18UCSC Ensembl
Outerchr15:30900566..30900613hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7765932, essv7769099, essv7766628
SamplesNA12873, NA12814, NA12045
Known GenesFMN1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3304136
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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