A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660775



Internal ID4705109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31823805..31827991hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv5815982, essv5922810
SamplesHG00553, HG00637
Known GenesDMD
Method
Analysis
Platform
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660775
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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