A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156177



Internal ID22086682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68494770..68640616hg38UCSC Ensembl
Outerchr4:68478894..68655691hg38UCSC Ensembl
Innerchr4:69360488..69506334hg19UCSC Ensembl
Outerchr4:69344612..69521409hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38176798
hg19176798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218n97
Supporting Variantsnssv4016700, nssv4016699
Samples
Known GenesTMPRSS11E, UGT2B15, UGT2B17
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156177
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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