A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809607



Internal ID13307544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154549595..154649599hg38UCSC Ensembl
InnerchrX:154551585..154648019hg38UCSC Ensembl
OuterchrX:154549485..154649719hg38UCSC Ensembl
chrX:153777810..153877873hg19UCSC Ensembl
InnerchrX:153779800..153876293hg19UCSC Ensembl
OuterchrX:153777700..153877993hg19UCSC Ensembl
chrX:153431004..153531067hg18UCSC Ensembl
InnerchrX:153432994..153529487hg18UCSC Ensembl
OuterchrX:153430894..153531187hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38100005
hg19100064
hg18100064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3369299
Supporting Variants
SamplesNA12878
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809607
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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