A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997196



Internal ID7081166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:75126775..75135311hg38UCSC Ensembl
Outerchr10:76886533..76895069hg19UCSC Ensembl
Outerchr10:76556539..76565075hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg388537
hg198537
hg188537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565570
SamplesHuRef
Known GenesSAMD8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997196
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