A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110572



Internal ID21293838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53365496..53369980hg38UCSC Ensembl
Innerchr17:51442857..51447341hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384485
hg194485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv500n145
Supporting Variantsnssv14098081, nssv14098532
Samplessample65, sample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110572
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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