A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117779



Internal ID21301045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54530217..54533197hg38UCSC Ensembl
InnerchrX:54556650..54559630hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104970
Samplessample148
Known GenesGNL3L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117779
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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