A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564014



Internal ID7035114
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011111
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564014
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer