A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008106



Internal ID7073200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:27880010..27889071hg38UCSC Ensembl
Outerchr17:26207036..26216097hg19UCSC Ensembl
Outerchr17:23231163..23240224hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389062
hg199062
hg189062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563580
SamplesHuRef
Known GenesLYRM9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008106
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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