A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660935



Internal ID9927040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:58139223..58173918hg38UCSC Ensembl
chrX:58165657..58200352hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3834696
hg1934696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5412279
SamplesHG00607
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660935
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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