A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004911



Internal ID7070007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:23552209..23553649hg38UCSC Ensembl
Outerchr10:23841138..23842578hg19UCSC Ensembl
Outerchr10:23881144..23882584hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383979
hg193979
hg183979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565749
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004911
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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