A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113437



Internal ID21296703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178723845..178727634hg38UCSC Ensembl
Innerchr1:178692980..178696769hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097569
Samplessample348
Known GenesRALGPS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113437
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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