A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4606e59



Internal ID22765826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115843163..115890089hg38UCSC Ensembl
chrX:114959496..115006422hg19UCSC Ensembl
chrX:114865752..114920450hg18UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3846927
hg1946927
hg1854699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3353697, esv3353476, esv3449595, esv3364679
SamplesNA19238, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4606e59
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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