A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104165



Internal ID21266700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:149499610..149572205hg38UCSC Ensembl
InnerchrX:148581141..148653739hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3872596
hg1972599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114085
Supporting Variants
Samplessample101
Known GenesCXorf40A, IDS, LINC00893
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104165
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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