A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663973



Internal ID9930078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65801041..65824226hg38UCSC Ensembl
chrX:65020883..65044068hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3823186
hg1923186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6543678
SamplesHG00369
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663973
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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