A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117266



Internal ID21300532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140956628..140994724hg38UCSC Ensembl
InnerchrX:140038793..140076889hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3838097
hg1938097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1283n145
Supporting Variantsnssv14105072
Samplessample223
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117266
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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