A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3362411



Internal ID15209389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1619959..1621857hg38UCSC Ensembl
InnerchrX:1620857..1620959hg38UCSC Ensembl
OuterchrX:1618959..1622857hg38UCSC Ensembl
chrX:1738852..1740750hg19UCSC Ensembl
InnerchrX:1739750..1739852hg19UCSC Ensembl
OuterchrX:1737852..1741750hg19UCSC Ensembl
chrX:1698852..1700750hg18UCSC Ensembl
InnerchrX:1699852..1699750hg18UCSC Ensembl
OuterchrX:1697852..1701750hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697532
SamplesNA19239
Known GenesASMT
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3362411
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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