A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101825



Internal ID21287196
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 StatusS
Merged Variantsnsv3113032
Supporting Variants
Samplessample399
Known GenesARMCX4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101825
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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