A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674816



Internal ID9940921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64009207..64024279hg38UCSC Ensembl
chrX:63229087..63244159hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3815073
hg1915073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5487696
SamplesHG00501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674816
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