A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110368



Internal ID21293634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225122422..225125070hg38UCSC Ensembl
Innerchr2:225987139..225989787hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv670n145
Supporting Variantsnssv14102477
Samplessample54
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110368
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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