A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093792



Internal ID21284745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:84432719..84440423hg38UCSC Ensembl
Innerchr12:84826498..84834202hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg387705
hg197705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111275
Supporting Variants
Samplessample364
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093792
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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