A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303900



Internal ID15150848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103437063..103437064hg38UCSC Ensembl
InnerchrX:103437038..103437089hg38UCSC Ensembl
OuterchrX:103437037..103437090hg38UCSC Ensembl
chrX:102691991..102691992hg19UCSC Ensembl
InnerchrX:102691966..102692017hg19UCSC Ensembl
OuterchrX:102691965..102692018hg19UCSC Ensembl
chrX:102578647..102578648hg18UCSC Ensembl
InnerchrX:102578673..102578622hg18UCSC Ensembl
OuterchrX:102578621..102578674hg18UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38285
hg19285
hg18285
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7763313, essv7756325, essv7744639, essv7758141, essv7741498, essv7741059, essv7745356, essv7750549, essv7744032, essv7746528
SamplesNA18510, NA18498, NA18871, NA18907, NA18912, NA19257, NA18858, NA19147, NA18517, NA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303900
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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