A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302857



Internal ID15149805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70776093..70776505hg38UCSC Ensembl
Innerchr10:70776193..70776405hg38UCSC Ensembl
Outerchr10:70775993..70776605hg38UCSC Ensembl
chr10:72535849..72536261hg19UCSC Ensembl
Innerchr10:72535949..72536161hg19UCSC Ensembl
Outerchr10:72535749..72536361hg19UCSC Ensembl
chr10:72205855..72206267hg18UCSC Ensembl
Innerchr10:72205955..72206167hg18UCSC Ensembl
Outerchr10:72205755..72206367hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38413
hg19413
hg18413
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7732919
SamplesNA18563
Known GenesTBATA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302857
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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