A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558708



Internal ID18759784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24284857..24285957hg38UCSC Ensembl
OuterchrX:24284708..24286087hg38UCSC Ensembl
InnerchrX:24302974..24304074hg19UCSC Ensembl
OuterchrX:24302825..24304204hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757455
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558708
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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