A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155825



Internal ID22086330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:50063167..50073927hg38UCSC Ensembl
Outerchr1:50062919..50077250hg38UCSC Ensembl
Innerchr1:50528839..50539599hg19UCSC Ensembl
Outerchr1:50528591..50542922hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3814332
hg1914332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015241
Samples
Known GenesELAVL4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155825
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