A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104136



Internal ID21291974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:25902892..25908209hg38UCSC Ensembl
InnerchrX:25921009..25926326hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg385318
hg195318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117081
Supporting Variants
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104136
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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