A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4561e59



Internal ID22765781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1293559..1298757hg38UCSC Ensembl
chrX:1412452..1417650hg19UCSC Ensembl
chrX:1372452..1377650hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385199
hg195199
hg185199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3417820, esv3356915
SamplesNA19239, NA19240
Known GenesCSF2RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4561e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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