A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559356



Internal ID18760432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134213971..134217400hg38UCSC Ensembl
OuterchrX:134213471..134218252hg38UCSC Ensembl
InnerchrX:133348001..133351430hg19UCSC Ensembl
OuterchrX:133347501..133352282hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg384782
hg194782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758103
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559356
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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