A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116443



Internal ID21299709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5007537..5047975hg38UCSC Ensembl
InnerchrX:4925578..4966016hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3840439
hg1940439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104973
Samplessample149
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116443
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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