A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8977921



Internal ID14018810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5863705..5863714hg38UCSC Ensembl
InnerchrX:5863698..5863721hg38UCSC Ensembl
OuterchrX:5863689..5863730hg38UCSC Ensembl
chrX:5781746..5781755hg19UCSC Ensembl
InnerchrX:5781739..5781762hg19UCSC Ensembl
OuterchrX:5781730..5781771hg19UCSC Ensembl
chrX:5791746..5791755hg18UCSC Ensembl
InnerchrX:5791762..5791739hg18UCSC Ensembl
OuterchrX:5791730..5791771hg18UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3406542
Supporting Variants
SamplesNA18550
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8977921
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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