A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115635



Internal ID21298901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:32875523..32879290hg38UCSC Ensembl
Innerchr17:31202541..31206308hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383768
hg193768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097631
Samplessample208
Known GenesMYO1D
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115635
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer