A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111166



Internal ID21294432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72556504..72562305hg38UCSC Ensembl
Innerchr9:75171420..75177221hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089529
Samplessample66
Known GenesTMC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111166
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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