A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110637



Internal ID21293903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62964825..62968071hg38UCSC Ensembl
Innerchr17:61042186..61045432hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg383247
hg193247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098881
Samplessample138
Known GenesMIR548W
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110637
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