A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116989



Internal ID21300255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135628535..135704679hg38UCSC Ensembl
InnerchrX:134762460..134838394hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3876145
hg1975935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1281n145
Supporting Variantsnssv14104172
Samplessample104
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116989
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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