A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111758



Internal ID21295024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27966310..27969362hg38UCSC Ensembl
InnerchrX:27984427..27987479hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg383053
hg193053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101649
Samplessample274
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111758
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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