A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328238



Internal ID15175223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46951443..46971212hg38UCSC Ensembl
InnerchrX:46952483..46969220hg38UCSC Ensembl
OuterchrX:46951443..46971306hg38UCSC Ensembl
chrX:46810899..46831206hg19UCSC Ensembl
InnerchrX:46812889..46829626hg19UCSC Ensembl
OuterchrX:46810789..46831326hg19UCSC Ensembl
chrX:46695843..46716150hg18UCSC Ensembl
InnerchrX:46697833..46714570hg18UCSC Ensembl
OuterchrX:46695733..46716270hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819770
hg1920308
hg1820308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4585e59
Supporting Variantsessv8809619
SamplesNA12878
Known GenesJADE3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328238
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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