A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305862



Internal ID15152810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8438170..8438171hg38UCSC Ensembl
Innerchr10:8438134..8438207hg38UCSC Ensembl
Outerchr10:8438133..8438208hg38UCSC Ensembl
chr10:8480133..8480134hg19UCSC Ensembl
Innerchr10:8480097..8480170hg19UCSC Ensembl
Outerchr10:8480096..8480171hg19UCSC Ensembl
chr10:8520139..8520140hg18UCSC Ensembl
Innerchr10:8520176..8520103hg18UCSC Ensembl
Outerchr10:8520102..8520177hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7749798, essv7740476, essv7761446, essv7755800, essv7740885
SamplesNA18504, NA19137, NA18499, NA19093, NA19102
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305862
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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