A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758259



Internal ID18732505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155057025..155057452hg38UCSC Ensembl
OuterchrX:155057015..155057496hg38UCSC Ensembl
InnerchrX:154285300..154285727hg19UCSC Ensembl
OuterchrX:154285290..154285771hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758259
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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