A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008495



Internal ID6720605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1368871..1368871hg38UCSC Ensembl
chr10:1411066..1411066hg19UCSC Ensembl
chr10:1401066..1401066hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38116
hg19116
hg18116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3578624
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008495
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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