A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113760



Internal ID21297026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54609874..54614067hg38UCSC Ensembl
Innerchr17:52687235..52691428hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384194
hg194194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098073, nssv14098068
Samplessample60, sample62
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113760
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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