A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020424



Internal ID22082055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109702376hg38UCSC Ensembl
Outerchr1:109697556..109703504hg38UCSC Ensembl
Innerchr1:110242954..110244998hg19UCSC Ensembl
Outerchr1:110240178..110246126hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385949
hg195949
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156473
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020424
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