A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114901



Internal ID21298167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53333209..53344586hg38UCSC Ensembl
Innerchr17:51410570..51421947hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811378
hg1911378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098963
Samplessample177
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114901
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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