A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809619



Internal ID13654386
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 StatusS
Merged Variantsesv3328238
Supporting Variants
SamplesNA12878
Known GenesJADE3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809619
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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