A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111726



Internal ID21294992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209936517..209941275hg38UCSC Ensembl
Innerchr1:210109862..210114620hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg384759
hg194759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109n145
Supporting Variantsnssv14091251
Samplessample296
Known GenesSYT14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111726
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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