A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009898



Internal ID6721990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:65139616..65150605hg38UCSC Ensembl
Outerchr17:63135734..63146723hg19UCSC Ensembl
Outerchr17:60566196..60577185hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3810990
hg1910990
hg1810990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564780
SamplesHuRef
Known GenesRGS9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009898
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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