A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559106



Internal ID18760182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94146200..94149716hg38UCSC Ensembl
OuterchrX:94145894..94149796hg38UCSC Ensembl
InnerchrX:93401199..93404715hg19UCSC Ensembl
OuterchrX:93400893..93404795hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383903
hg193903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757853
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559106
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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