A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758128



Internal ID18732374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138282589..138283029hg38UCSC Ensembl
OuterchrX:138282577..138283055hg38UCSC Ensembl
InnerchrX:137364748..137365188hg19UCSC Ensembl
OuterchrX:137364736..137365214hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758128
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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