A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757599



Internal ID18385159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233763..47233816hg38UCSC Ensembl
chrX:47093162..47093215hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558852
Supporting Variants
Samples
Known GenesUSP11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757599
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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