A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757590



Internal ID18731836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45184079..45203995hg38UCSC Ensembl
OuterchrX:45183256..45205255hg38UCSC Ensembl
InnerchrX:45043324..45063240hg19UCSC Ensembl
OuterchrX:45042501..45064500hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3822000
hg1922000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558843
Supporting Variants
Samples
Known GenesCXorf36
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757590
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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