A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305614



Internal ID15152562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75469288..75469289hg38UCSC Ensembl
Innerchr10:75469270..75469307hg38UCSC Ensembl
Outerchr10:75469269..75469308hg38UCSC Ensembl
chr10:77229046..77229047hg19UCSC Ensembl
Innerchr10:77229028..77229065hg19UCSC Ensembl
Outerchr10:77229027..77229066hg19UCSC Ensembl
chr10:76899052..76899053hg18UCSC Ensembl
Innerchr10:76899071..76899034hg18UCSC Ensembl
Outerchr10:76899033..76899072hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38309
hg19309
hg18309
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7777556, essv7781102, essv7829098, essv7831155, essv7827496, essv7810806, essv7830357, essv7810078, essv7808771, essv7793368, essv7776929, essv7830488, essv7823681, essv7834248, essv7826913, essv7773651, essv7787909, essv7796739, essv7820927, essv7779121, essv7786725, essv7788122, essv7814321
SamplesNA18980, NA11931, NA18959, NA18558, NA18942, NA11918, NA18582, NA12287, NA18964, NA12044, NA18973, NA18638, NA18951, NA18956, NA12249, NA18593, NA18608, NA18952, NA18943, NA12749, NA18552, NA12154, NA18965
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305614
Frequency
Sample Size185
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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