A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564662



Internal ID7035762
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002111
Supporting Variants
SamplesHuRef
Known GenesMSI2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564662
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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