A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661336



Internal ID9927441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:819814..867357hg38UCSC Ensembl
chrX:780549..828092hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3847544
hg1947544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6017039, essv6511289
SamplesHG01070, NA19780
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661336
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