A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002111



Internal ID7067229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57557056..57567738hg38UCSC Ensembl
Outerchr17:55634417..55645099hg19UCSC Ensembl
Outerchr17:52989416..53000098hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810683
hg1910683
hg1810683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564662
SamplesHuRef
Known GenesMSI2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002111
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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