A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3408326



Internal ID15255288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10967412..10967434hg38UCSC Ensembl
Innerchr10:10967420..10967424hg38UCSC Ensembl
Outerchr10:10967400..10967446hg38UCSC Ensembl
chr10:11009375..11009397hg19UCSC Ensembl
Innerchr10:11009383..11009387hg19UCSC Ensembl
Outerchr10:11009363..11009409hg19UCSC Ensembl
chr10:11049381..11049403hg18UCSC Ensembl
Innerchr10:11049393..11049389hg18UCSC Ensembl
Outerchr10:11049369..11049415hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38224
hg19224
hg18224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8946968, essv8946971, essv8946970
SamplesNA18907, NA19257, NA19147
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3408326
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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