A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688147



Internal ID15040865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88092315..88094413hg38UCSC Ensembl
Innerchr10:88093315..88093413hg38UCSC Ensembl
Outerchr10:88091315..88095413hg38UCSC Ensembl
chr10:89852072..89854170hg19UCSC Ensembl
Innerchr10:89853072..89853170hg19UCSC Ensembl
Outerchr10:89851072..89855170hg19UCSC Ensembl
chr10:89842052..89844150hg18UCSC Ensembl
Innerchr10:89843052..89843150hg18UCSC Ensembl
Outerchr10:89841052..89845150hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3387445
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688147
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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