A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559352



Internal ID18760428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:133524161..133529259hg38UCSC Ensembl
OuterchrX:133523973..133529472hg38UCSC Ensembl
InnerchrX:132658189..132663287hg19UCSC Ensembl
OuterchrX:132658001..132663500hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758099
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559352
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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