A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106036



Internal ID21279775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:179859219..179863619hg38UCSC Ensembl
Innerchr2:180723946..180728346hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112779
Supporting Variants
Samplessample289
Known GenesMIR1258, ZNF385B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106036
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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