A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113404



Internal ID21296670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154750007..154752596hg38UCSC Ensembl
InnerchrX:153978282..153980871hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382590
hg192590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105056
Samplessample208
Known GenesGAB3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113404
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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