A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4621e59



Internal ID22765841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135944927..135946325hg38UCSC Ensembl
chrX:135027086..135028484hg19UCSC Ensembl
chrX:134854752..134856150hg18UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3414226, esv3350177
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4621e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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