A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155461



Internal ID22085966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10310483..10317925hg38UCSC Ensembl
Outerchr1:10307286..10321714hg38UCSC Ensembl
Innerchr1:10370541..10377983hg19UCSC Ensembl
Outerchr1:10367344..10381772hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3814429
hg1914429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012214
Samples
Known GenesKIF1B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155461
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