A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559164



Internal ID18413554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:104157745..104158346hg38UCSC Ensembl
OuterchrX:104157733..104158364hg38UCSC Ensembl
InnerchrX:103402426..103403027hg19UCSC Ensembl
OuterchrX:103402414..103403045hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757911
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559164
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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