A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669681



Internal ID9935786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111564551..111564965hg38UCSC Ensembl
chrX:110807779..110808193hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6312527, essv6257318
SamplesNA18858, NA19213
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669681
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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