A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116891



Internal ID21300157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209935183..209940617hg38UCSC Ensembl
Innerchr1:210108528..210113962hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg385435
hg195435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109n145
Supporting Variantsnssv14101468
Samplessample397
Known GenesSYT14
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116891
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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