A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328612



Internal ID15175599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8438162..8438192hg38UCSC Ensembl
Innerchr10:8438174..8438178hg38UCSC Ensembl
Outerchr10:8438144..8438208hg38UCSC Ensembl
chr10:8480125..8480155hg19UCSC Ensembl
Innerchr10:8480137..8480141hg19UCSC Ensembl
Outerchr10:8480107..8480171hg19UCSC Ensembl
chr10:8520131..8520161hg18UCSC Ensembl
Innerchr10:8520147..8520143hg18UCSC Ensembl
Outerchr10:8520113..8520177hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38249
hg19249
hg18249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8946718, essv8946715, essv8946716, essv8946713, essv8946717
SamplesNA18504, NA19137, NA18499, NA19093, NA19102
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328612
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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