A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113032



Internal ID21296298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101424794..101433691hg38UCSC Ensembl
InnerchrX:100679782..100688679hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg388898
hg198898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101825
Samplessample399
Known GenesARMCX4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113032
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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