A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113403



Internal ID21296669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:16303456..16396701hg38UCSC Ensembl
InnerchrX:16321579..16414824hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3893246
hg1993246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104113
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113403
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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