A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665694



Internal ID9931799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27905094..27905417hg38UCSC Ensembl
chrX:27923211..27923534hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6372057, essv5926915, essv6210970, essv5905186, essv6140440, essv5627105, essv6425946, essv6059065, essv5416175, essv5759325
SamplesNA19700, NA19332, NA18486, NA18870, NA19920, NA19373, NA19437, NA19452, NA19440, NA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665694
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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