A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104102



Internal ID21289959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7859794..8085636hg38UCSC Ensembl
InnerchrX:7827835..8053677hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38225843
hg19225843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111588
Supporting Variants
Samplessample53
Known GenesPNPLA4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104102
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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