A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757837



Internal ID18732083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:90323370..90325359hg38UCSC Ensembl
OuterchrX:90323222..90325535hg38UCSC Ensembl
InnerchrX:89578369..89580358hg19UCSC Ensembl
OuterchrX:89578221..89580534hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382314
hg192314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757837
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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