A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105961



Internal ID21268991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112244772..112247578hg38UCSC Ensembl
Innerchr3:111963619..111966425hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382807
hg192807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111500
Supporting Variants
Samplessample133
Known GenesSLC9C1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105961
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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