A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558892



Internal ID18759968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:55676766..55682567hg38UCSC Ensembl
OuterchrX:55675068..55683567hg38UCSC Ensembl
InnerchrX:55703199..55709000hg19UCSC Ensembl
OuterchrX:55701501..55710000hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757639
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558892
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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