A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117082



Internal ID21300348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118224477..118231310hg38UCSC Ensembl
InnerchrX:117358440..117365273hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg386834
hg196834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1274n145
Supporting Variantsnssv14104939
Samplessample125
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117082
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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