A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865013



Internal ID13317708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35739850..35739861hg38UCSC Ensembl
Innerchr10:35739852..35739859hg38UCSC Ensembl
Outerchr10:35739848..35739863hg38UCSC Ensembl
chr10:36028778..36028789hg19UCSC Ensembl
Innerchr10:36028780..36028787hg19UCSC Ensembl
Outerchr10:36028776..36028791hg19UCSC Ensembl
chr10:36068784..36068795hg18UCSC Ensembl
Innerchr10:36068786..36068793hg18UCSC Ensembl
Outerchr10:36068782..36068797hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3435069
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865013
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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