A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113775



Internal ID21297041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151388779..151419218hg38UCSC Ensembl
Innerchr5:150768340..150798779hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3830440
hg1930440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv996n145
Supporting Variantsnssv14108453
Samplessample150
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113775
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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