A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156199



Internal ID22086704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90935503..90977919hg38UCSC Ensembl
Outerchr4:90931644..90982717hg38UCSC Ensembl
Innerchr4:91856654..91899070hg19UCSC Ensembl
Outerchr4:91852795..91903868hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3851074
hg1951074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014719
Samples
Known GenesCCSER1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156199
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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