A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090202



Internal ID21279540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248591107..248632837hg38UCSC Ensembl
Innerchr1:248754408..248796138hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3841731
hg1941731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110794
Supporting Variants
Samplessample285
Known GenesOR2T10, OR2T11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090202
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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