A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757859



Internal ID18732105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94778425..94830403hg38UCSC Ensembl
OuterchrX:94775502..94834895hg38UCSC Ensembl
InnerchrX:94033424..94085402hg19UCSC Ensembl
OuterchrX:94030501..94089894hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3859394
hg1959394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757859
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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