A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758184



Internal ID18732430
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 StatusS
Merged Variantsesv3559437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758184
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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