A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115237



Internal ID21298503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169246873..169271567hg38UCSC Ensembl
Innerchr1:169216111..169240805hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3824695
hg1924695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv82n145
Supporting Variantsnssv14090172, nssv14093918, nssv14083251, nssv14091207, nssv14106123, nssv14100286, nssv14107506
Samplessample60, sample384, sample260, sample105, sample308, sample296, sample187
Known GenesNME7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115237
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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