A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154339



Internal ID22084844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169264736..169272528hg38UCSC Ensembl
Outerchr1:169247699..169273163hg38UCSC Ensembl
Innerchr1:169233974..169241766hg19UCSC Ensembl
Outerchr1:169216937..169242401hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3825465
hg1925465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022993, nssv4005150, nssv4005168, nssv4005167, nssv4005160, nssv4005158, nssv4022991, nssv4005151, nssv4005153, nssv4005149, nssv4005156, nssv4023001, nssv4023002, nssv4022998, nssv4005155, nssv4022999, nssv4005170, nssv4005166, nssv4022979, nssv4022990, nssv4022988, nssv4022986, nssv4005159, nssv4022984, nssv4022977, nssv4005157, nssv4005163, nssv4005154, nssv4022981, nssv4022989, nssv4022982, nssv4022997, nssv4005165, nssv4023000, nssv4022987, nssv4005169, nssv4022995, nssv4022992, nssv4022983, nssv4022994, nssv4022978, nssv4005171, nssv4005164, nssv4022985, nssv4005162, nssv4005152, nssv4022996, nssv4022980, nssv4005161
Samples
Known GenesNME7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154339
Frequency
Sample Size131
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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