A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558926



Internal ID18413316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:65711046..65711208hg38UCSC Ensembl
OuterchrX:65711010..65711220hg38UCSC Ensembl
InnerchrX:64930908..64931070hg19UCSC Ensembl
OuterchrX:64930872..64931082hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757673
Samples
Known GenesMSN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558926
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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