A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105096



Internal ID21276704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:78651114..78654327hg38UCSC Ensembl
InnerchrX:77906611..77909824hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg383214
hg193214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116707
Supporting Variants
Samplessample240
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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