A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758142



Internal ID18732388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139963644..139963765hg38UCSC Ensembl
OuterchrX:139963637..139963771hg38UCSC Ensembl
InnerchrX:139045803..139045924hg19UCSC Ensembl
OuterchrX:139045796..139045930hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559395
Supporting Variants
Samples
Known GenesCXorf66
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758142
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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