A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093239



Internal ID21279458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248591107..248625382hg38UCSC Ensembl
Innerchr1:248754408..248788683hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3834276
hg1934276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116125
Supporting Variants
Samplessample283
Known GenesOR2T10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093239
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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