A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7740885



Internal ID14896009
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 StatusS
Merged Variantsesv3305862
Supporting Variants
SamplesNA19137
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7740885
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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