A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3323542



Internal ID15170517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157255..49162735hg38UCSC Ensembl
InnerchrX:49158613..49160745hg38UCSC Ensembl
OuterchrX:49157255..49162845hg38UCSC Ensembl
chrX:49013844..49019548hg19UCSC Ensembl
InnerchrX:49015834..49017968hg19UCSC Ensembl
OuterchrX:49013734..49019668hg19UCSC Ensembl
chrX:48900788..48906492hg18UCSC Ensembl
InnerchrX:48902778..48904912hg18UCSC Ensembl
OuterchrX:48900678..48906612hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385481
hg195705
hg185705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4588e59
Supporting Variantsessv8809622
SamplesNA12878
Known GenesMAGIX
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3323542
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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