A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093723



Internal ID21283421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:82675142..82682252hg38UCSC Ensembl
Innerchr12:83068921..83076031hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg387111
hg197111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116012
Supporting Variants
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093723
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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