A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4576e59



Internal ID22765796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30788314..30799712hg38UCSC Ensembl
chrX:30806431..30817829hg19UCSC Ensembl
chrX:30716352..30727750hg18UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3811399
hg1911399
hg1811399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3336867, esv3327969
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4576e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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