A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559482



Internal ID18760558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152462529..152475744hg38UCSC Ensembl
OuterchrX:152462291..152476028hg38UCSC Ensembl
InnerchrX:151631001..151644216hg19UCSC Ensembl
OuterchrX:151630763..151644500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813738
hg1913738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758229
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559482
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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