A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992380



Internal ID7062106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39165445..39165445hg38UCSC Ensembl
chr11:39186995..39186995hg19UCSC Ensembl
chr11:39143571..39143571hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3881
hg1981
hg1881
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3569728
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992380
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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