A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104995



Internal ID21271398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34970259..35320730hg38UCSC Ensembl
InnerchrX:34988376..35338847hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38350472
hg19350472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117103
Supporting Variants
Samplessample163
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104995
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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