A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110135



Internal ID21293401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44101840..44105264hg38UCSC Ensembl
InnerchrX:43961086..43964510hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105054
Samplessample208
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110135
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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