A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091235



Internal ID21272934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:43636651..43649657hg38UCSC Ensembl
Innerchr12:44030454..44043460hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3813007
hg1913007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115550
Supporting Variants
Samplessample184
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091235
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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