A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101701



Internal ID21281105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115565922..115569558hg38UCSC Ensembl
InnerchrX:114800248..114803874hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383637
hg193627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112275
Supporting Variants
Samplessample307
Known GenesPLS3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101701
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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