A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559437



Internal ID18760513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:146861683..146862423hg38UCSC Ensembl
OuterchrX:146861555..146862516hg38UCSC Ensembl
InnerchrX:145943201..145943941hg19UCSC Ensembl
OuterchrX:145943073..145944034hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758184
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559437
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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