A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104056



Internal ID21279242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112918171..112922125hg38UCSC Ensembl
InnerchrX:112161399..112165353hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111918
Supporting Variants
Samplessample28
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104056
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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