A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112972



Internal ID21296238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21040786..21045047hg38UCSC Ensembl
Innerchr17:20944099..20948360hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384262
hg194262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098088
Samplessample69
Known GenesUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112972
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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