A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305889



Internal ID15152837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:126426568..126426569hg38UCSC Ensembl
InnerchrX:126426510..126426627hg38UCSC Ensembl
OuterchrX:126426509..126426628hg38UCSC Ensembl
chrX:125560551..125560552hg19UCSC Ensembl
InnerchrX:125560493..125560610hg19UCSC Ensembl
OuterchrX:125560492..125560611hg19UCSC Ensembl
chrX:125388232..125388233hg18UCSC Ensembl
InnerchrX:125388291..125388174hg18UCSC Ensembl
OuterchrX:125388173..125388292hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3875
hg1975
hg1875
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7746518, essv7756137, essv7761427, essv7759887
SamplesNA18870, NA19172, NA18499, NA18858
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305889
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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