A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002915



Internal ID7068027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110907076..110907313hg38UCSC Ensembl
chr13:111559423..111559660hg19UCSC Ensembl
chr13:110357424..110357661hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38238
hg19238
hg18238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3567843
SamplesHuRef
Known GenesANKRD10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002915
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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