A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117664



Internal ID21300930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244334040..244339098hg38UCSC Ensembl
Innerchr1:244497342..244502400hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14084031
Samplessample180
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117664
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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