A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675065



Internal ID9941170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103554035..103571451hg38UCSC Ensembl
chrX:102808963..102826379hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3817417
hg1917417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5551904, essv5985378
SamplesNA20543, NA11892
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675065
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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