A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116019



Internal ID21299285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30299446..30303604hg38UCSC Ensembl
InnerchrX:30317563..30321721hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg384159
hg194159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1262n145
Supporting Variantsnssv14104187, nssv14101685, nssv14105044
Samplessample200, sample300, sample117
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116019
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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