A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8949574



Internal ID14355129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:81106353..81106387hg38UCSC Ensembl
Innerchr10:81106357..81106381hg38UCSC Ensembl
Outerchr10:81106325..81106415hg38UCSC Ensembl
chr10:82866109..82866143hg19UCSC Ensembl
Innerchr10:82866113..82866137hg19UCSC Ensembl
Outerchr10:82866081..82866171hg19UCSC Ensembl
chr10:82856089..82856123hg18UCSC Ensembl
Innerchr10:82856117..82856093hg18UCSC Ensembl
Outerchr10:82856061..82856151hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38282
hg19282
hg18282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3360056
Supporting Variants
SamplesNA18856
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8949574
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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