A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7426690



Internal ID10704972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:39324005..39324531hg38UCSC Ensembl
Outerchr17:37480258..37480784hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3157123
Supporting Variants
SamplesHuRef
Known GenesFBXL20
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7426690
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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