A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559381



Internal ID18760457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138282589..138283029hg38UCSC Ensembl
OuterchrX:138282577..138283055hg38UCSC Ensembl
InnerchrX:137364748..137365188hg19UCSC Ensembl
OuterchrX:137364736..137365214hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758128
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559381
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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