A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156386



Internal ID22086787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:138472272..138481268hg38UCSC Ensembl
Outerchr5:138469431..138482888hg38UCSC Ensembl
Innerchr5:137807961..137816957hg19UCSC Ensembl
Outerchr5:137805120..137818577hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3813458
hg1913458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234n97
Supporting Variantsnssv4020211, nssv4020212
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156386
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