A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113961



Internal ID21297227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138931457..139077985hg38UCSC Ensembl
InnerchrX:138013619..138160147hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38146529
hg19146529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101779
Samplessample363
Known GenesFGF13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113961
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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