A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117336



Internal ID21300602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248574916..248631260hg38UCSC Ensembl
Innerchr1:248738217..248794561hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3856345
hg1956345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n145
Supporting Variantsnssv14107995
Samplessample92
Known GenesOR2T10, OR2T11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117336
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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