A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3395816



Internal ID15242780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26782302..26792690hg38UCSC Ensembl
InnerchrX:26784292..26791110hg38UCSC Ensembl
OuterchrX:26782192..26792810hg38UCSC Ensembl
chrX:26800419..26810807hg19UCSC Ensembl
InnerchrX:26802409..26809227hg19UCSC Ensembl
OuterchrX:26800309..26810927hg19UCSC Ensembl
chrX:26710340..26720728hg18UCSC Ensembl
InnerchrX:26712330..26719148hg18UCSC Ensembl
OuterchrX:26710230..26720848hg18UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3810389
hg1910389
hg1810389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809612
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3395816
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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