A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115120



Internal ID21298386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178922463..178925787hg38UCSC Ensembl
Innerchr1:178891598..178894922hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg383325
hg193325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097109
Samplessample349
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115120
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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