A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104930



Internal ID21267865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43652652..43656655hg38UCSC Ensembl
InnerchrX:43511900..43515903hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg384004
hg194004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113199
Supporting Variants
Samplessample118
Known GenesMAOA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104930
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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