A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556995



Internal ID18411385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31773346..31773436hg38UCSC Ensembl
chr20:30361149..30361239hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755742
Samples
Known GenesTPX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556995
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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