A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8946717



Internal ID14809739
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 StatusS
Merged Variantsesv3328612
Supporting Variants
SamplesNA19093
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8946717
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer