A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091697



Internal ID21280131
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 StatusS
Merged Variantsnsv3113320
Supporting Variants
Samplessample293
Known GenesNME7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091697
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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