A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3423659



Internal ID14923930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1473947..1473947hg38UCSC Ensembl
Innerchr10:1473946..1473948hg38UCSC Ensembl
Outerchr10:1473897..1473997hg38UCSC Ensembl
chr10:1516142..1516142hg19UCSC Ensembl
Innerchr10:1516141..1516143hg19UCSC Ensembl
Outerchr10:1516092..1516192hg19UCSC Ensembl
chr10:1506142..1506142hg18UCSC Ensembl
Innerchr10:1506143..1506141hg18UCSC Ensembl
Outerchr10:1506092..1506192hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8701258
SamplesNA12878
Known GenesADARB2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3423659
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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