A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111958



Internal ID21295224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125196042..125202576hg38UCSC Ensembl
Innerchr3:124914886..124921420hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg386535
hg196535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106508
Samplessample157
Known GenesSLC12A8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111958
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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