A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559328



Internal ID18413718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:129991298..129991785hg38UCSC Ensembl
OuterchrX:129991224..129991844hg38UCSC Ensembl
InnerchrX:129125274..129125761hg19UCSC Ensembl
OuterchrX:129125200..129125820hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758075
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559328
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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