A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092723



Internal ID21267338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:42627139..42635779hg38UCSC Ensembl
Innerchr12:43020941..43029581hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg388641
hg198641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116987
Supporting Variants
Samplessample111
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092723
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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