A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656672



Internal ID9922777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80060583..80069096hg38UCSC Ensembl
chrX:79316082..79324595hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg388514
hg198514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6141906
SamplesNA12058
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656672
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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