A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559519



Internal ID18413909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155560527..155560768hg38UCSC Ensembl
OuterchrX:155560499..155560800hg38UCSC Ensembl
InnerchrX:154790188..154790429hg19UCSC Ensembl
OuterchrX:154790160..154790461hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758266
Samples
Known GenesTMLHE
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559519
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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