A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660775



Internal ID2893862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31805688..31809874hg38UCSC Ensembl
chrX:31823805..31827991hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg384187
hg194187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5815982, essv5922810
SamplesHG00553, HG00637
Known GenesDMD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660775
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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