A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8809603



Internal ID13307423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14710450..14712785hg38UCSC Ensembl
InnerchrX:14711205..14712440hg38UCSC Ensembl
OuterchrX:14710340..14712905hg38UCSC Ensembl
chrX:14728572..14730907hg19UCSC Ensembl
InnerchrX:14729327..14730562hg19UCSC Ensembl
OuterchrX:14728462..14731027hg19UCSC Ensembl
chrX:14638493..14640828hg18UCSC Ensembl
InnerchrX:14640483..14639248hg18UCSC Ensembl
OuterchrX:14638383..14640948hg18UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382336
hg192336
hg182336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3435574
Supporting Variants
SamplesNA12878
Known GenesGLRA2
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8809603
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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