A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113320



Internal ID21296586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169246867..169271567hg38UCSC Ensembl
Innerchr1:169216105..169240805hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3824701
hg1924701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv82n145
Supporting Variantsnssv14091697, nssv14093763
Samplessample293, sample304
Known GenesNME7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113320
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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