A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006260



Internal ID6718378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131392221..131392221hg38UCSC Ensembl
chr11:131262116..131262116hg19UCSC Ensembl
chr11:130767326..130767326hg18UCSC Ensembl
Cytoband11q25
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 Variantsessv3579495
SamplesHuRef
Known GenesNTM
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006260
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer