A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758099



Internal ID18732345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:133524161..133529259hg38UCSC Ensembl
OuterchrX:133523973..133529472hg38UCSC Ensembl
InnerchrX:132658189..132663287hg19UCSC Ensembl
OuterchrX:132658001..132663500hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758099
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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