A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092880



Internal ID21270300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95788088..95791847hg38UCSC Ensembl
Innerchr12:96181866..96185625hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383760
hg193760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110741
Supporting Variants
Samplessample149
Known GenesNTN4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092880
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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