A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112786



Internal ID21296052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76551985..76626138hg38UCSC Ensembl
InnerchrX:75772394..75846547hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3874154
hg1974154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104151
Samplessample89
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112786
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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