A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088126



Internal ID21283718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68703704..68706947hg38UCSC Ensembl
Innerchr9:71318620..71321863hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383244
hg193244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114320
Supporting Variants
Samplessample349
Known GenesPIP5K1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088126
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