A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154421



Internal ID22084926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8009205..8017065hg38UCSC Ensembl
Outerchr9:8001166..8020572hg38UCSC Ensembl
Innerchr9:8009205..8017065hg19UCSC Ensembl
Outerchr9:8001166..8020572hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3819407
hg1919407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006124
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154421
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