A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3424547



Internal ID15271504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26782003..26803444hg38UCSC Ensembl
InnerchrX:26783993..26801864hg38UCSC Ensembl
OuterchrX:26781893..26803564hg38UCSC Ensembl
chrX:26800120..26821561hg19UCSC Ensembl
InnerchrX:26802110..26819981hg19UCSC Ensembl
OuterchrX:26800010..26821681hg19UCSC Ensembl
chrX:26710041..26731482hg18UCSC Ensembl
InnerchrX:26712031..26729902hg18UCSC Ensembl
OuterchrX:26709931..26731602hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3821442
hg1921442
hg1821442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809611
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3424547
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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