A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114136



Internal ID21297402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207209439..207217068hg38UCSC Ensembl
Innerchr2:208074163..208081792hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg387630
hg197630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104662
Samplessample145
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114136
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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