A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564642



Internal ID6689338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57604821..57614603hg38UCSC Ensembl
Outerchr17:55682182..55691964hg19UCSC Ensembl
Outerchr17:53037181..53046963hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg389783
hg199783
hg189783
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988833
Supporting Variants
SamplesHuRef
Known GenesMSI2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564642
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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