A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4563e59



Internal ID22765783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1446759..1448957hg38UCSC Ensembl
chrX:1565652..1567850hg19UCSC Ensembl
chrX:1525652..1527850hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3364881, esv3434986
SamplesNA19239, NA19240
Known GenesASMTL
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4563e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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