A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104079



Internal ID21289393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95058165..95124727hg38UCSC Ensembl
InnerchrX:94313164..94379726hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3866563
hg1966563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114644
Supporting Variants
Samplessample46
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104079
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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