A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558857



Internal ID18413247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:47506780..47521860hg38UCSC Ensembl
OuterchrX:47505404..47522364hg38UCSC Ensembl
InnerchrX:47366179..47381259hg19UCSC Ensembl
OuterchrX:47364803..47381763hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3816961
hg1916961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757604
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558857
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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