A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112961



Internal ID21296227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31430112..31436654hg38UCSC Ensembl
InnerchrX:31448229..31454771hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg386543
hg196543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104966
Samplessample146
Known GenesDMD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112961
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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