A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8949895



Internal ID13820840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94334811..94334835hg38UCSC Ensembl
Innerchr10:94334812..94334832hg38UCSC Ensembl
Outerchr10:94334788..94334856hg38UCSC Ensembl
chr10:96094568..96094592hg19UCSC Ensembl
Innerchr10:96094569..96094589hg19UCSC Ensembl
Outerchr10:96094545..96094613hg19UCSC Ensembl
chr10:96084558..96084582hg18UCSC Ensembl
Innerchr10:96084579..96084559hg18UCSC Ensembl
Outerchr10:96084535..96084603hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3407687
Supporting Variants
SamplesNA18505
Known GenesNOC3L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8949895
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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