A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117886



Internal ID21301152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84572600..84575294hg38UCSC Ensembl
Innerchr1:85038283..85040977hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg382695
hg192695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083500, nssv14095311, nssv14105422
Samplessample156, sample32, sample79
Known GenesCTBS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117886
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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