A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155218



Internal ID22085723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98454544..98465618hg38UCSC Ensembl
Outerchr15:98452871..98475189hg38UCSC Ensembl
Innerchr15:98997773..99008847hg19UCSC Ensembl
Outerchr15:98996100..99018418hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3822319
hg1922319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010474
Samples
Known GenesFAM169B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155218
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