A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307857



Internal ID15154805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94334808..94334809hg38UCSC Ensembl
Innerchr10:94334774..94334843hg38UCSC Ensembl
Outerchr10:94334773..94334844hg38UCSC Ensembl
chr10:96094565..96094566hg19UCSC Ensembl
Innerchr10:96094531..96094600hg19UCSC Ensembl
Outerchr10:96094530..96094601hg19UCSC Ensembl
chr10:96084555..96084556hg18UCSC Ensembl
Innerchr10:96084590..96084521hg18UCSC Ensembl
Outerchr10:96084520..96084591hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7749733, essv7743858, essv7750475, essv7752835
SamplesNA19257, NA19093, NA18505, NA18511
Known GenesNOC3L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307857
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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