A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096819



Internal ID21269354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2397118..2403263hg38UCSC Ensembl
Innerchr1:2328557..2334702hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg386146
hg196146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115383
Supporting Variants
Samplessample138
Known GenesRER1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096819
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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