A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011111



Internal ID7059873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:81840760..81847341hg38UCSC Ensembl
OuterchrX:81096259..81102840hg19UCSC Ensembl
OuterchrX:80982915..80989496hg18UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg386582
hg196582
hg186582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564014
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011111
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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